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Watchlist
Account
Femasys
FEMY
#10305
Rank
A$31.98 M
Marketcap
๐บ๐ธ
United States
Country
A$0.53
Share price
0.42%
Change (1 day)
-67.89%
Change (1 year)
Medical devices
Categories
Market cap
Revenue
Earnings
Price history
P/E ratio
P/S ratio
More
Price history
P/E ratio
P/S ratio
P/B ratio
Operating margin
EPS
Shares outstanding
Fails to deliver
Cost to borrow
Total assets
Total liabilities
Total debt
Cash on Hand
Net Assets
Annual Reports (10-K)
Femasys
Quarterly Reports (10-Q)
Submitted on 2026-05-08
Femasys - 10-Q quarterly report FY
Text size:
Small
Medium
Large
UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
Washington, D.C. 20549
FORM
10-Q
(Mark One)
☑
QUARTERLY REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934
For the quarterly period ended
March 31,
2026
OR
☐
TRANSITION REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934
For the transition period from ____________to____________
Commission file number:
001-40492
.
Femasys Inc.
(Exact Name of Registrant as Specified in its Charter)
Delaware
11-3713499
(State or other jurisdiction of incorporation or organization)
(IRS Employer Identification No.)
3950 Johns Creek Court
,
Suite 100
Suwanee
,
GA
30024
(Address of principal executive offices)
(Zip Code)
(
770
)
500-3910
(Registrant’s telephone number, including area code)
N/A
(Former name, former address and former fiscal year, if changed since last report)
Securities registered pursuant to Section 12(b) of the Act:
Title of each class
Trading symbol
Name of each exchange on
which
Registered
Common stock, $0.001 par value
FEMY
The
Nasdaq
Capital Market
Indicate by check mark whether the registrant (1) has filed all reports required to be filed by Section 13 or 15(d) of the Securities Exchange Act of 1934 during the preceding 12 months (or for such shorter period that the registrant was required to file such reports), and (2) has been subject to such filing requirements for the past 90 days.
Yes
☑ No ☐
Indicate by check mark whether the registrant has submitted electronically every Interactive Data File required to be submitted pursuant to Rule 405 of Regulation S-T during the preceding 12 months (or for such shorter period that the registrant was required to submit such files).
Yes
☑ No ☐
Indicate by check mark whether the registrant is a large accelerated filer, an accelerated filer, a non-accelerated filer, or a smaller reporting company, or an emerging growth company. See the definitions of “large accelerated filer,” “accelerated filer” and “smaller reporting company” and “emerging growth company” in Rule 12b-2 of the Exchange Act.
Large accelerated filer ☐
Accelerated filer ☐
Non-accelerated filer
☑
Smaller reporting company
☑
Emerging growth company
☑
If an emerging growth company, indicate by check mark if the registrant has elected not to use the extended transition period for complying with any new or revised financial accounting standards provided pursuant to Section 13(a) of the Exchange Act.
☑
Indicate by check mark whether the registrant is a shell company (as defined in Rule 12b-2 of the Exchange Act). Yes ☐ No
☑
The Registrant had
60,390,686
shares of common stock, $0.001 par value, outstanding as of May 7, 2026.
1
TABLE OF CONTENTS
Page
Part I. Financial Information
Item 1
Condensed Financial Statements
5
Condensed Balance Sheets as of March 31, 2026 and December 31, 2025 (unaudited)
6
Condensed Statements of Comprehensive Income (Loss) for the Three Months Ended March 31, 2026 and 2025 (unaudited)
7
Condensed Statements of Stockholders’ Equity for the Three Months Ended March 31, 2026 and 2025 (unaudited)
8
Condensed Statements of Cash Flows for the Three Months Ended March 31, 2026 and 2025 (unaudited)
9
Notes to Condensed Financial Statements (unaudited)
10
Item 2
Management’s Discussion and Analysis of Financial Condition and Results of Operations
28
Item 3
Quantitative and Qualitative Disclosures About Market Risk
38
Item 4
Controls and Procedures
39
Part II. Other Information
Item 1
Legal Proceedings
39
Item 1A
Risk Factors
39
Item 2
Unregistered Sales of Equity Securities and Use of Proceeds
42
Item 3
Defaults Upon Senior Securities
42
Item 4
Mine Safety Disclosures
42
Item 5
Other Information
42
Item 6
Exhibits
43
SIGNATURES
2
Table of Contents
SPECIAL NOTE REGARDING FORWARD-LOOKING STATEMENTS
This Quarterly Report on Form 10-Q contains forward-looking statements. All statements other than statements of historical facts contained in this Quarterly Report on Form 10-Q are forward-looking statements. In some cases, you can identify forward-looking statements by terms such as “may,” “will,” “should,” “expect,” “plan,” “anticipate,” “could,” “intend,” “target,” “project,” “contemplate,” “believe,” “estimate,” “predict,” “potential” or “continue” or the negative of these terms or other similar expressions, although not all forward-looking statements contain these words. Forward-looking statements include, but are not limited to, statements concerning:
• our ability to obtain additional financing to fund commercialization of our products and fund our operations;
• our ability to obtain additional financing to fund the U.S. clinical development of our U.S. product candidate FemBloc® permanent birth control;
• our ability to obtain U.S. Food and Drug Administration (FDA) approval for our U.S. product candidate, FemBloc for permanent birth control;
• our ability to successfully grow sales of FemaSeed® intratubal insemination in the U.S.;
• our ability to successfully grow sales internationally;
• estimates regarding the total addressable market for our products and U.S. product candidate;
• competitive companies and technologies in our industry;
• our business model and strategic plans for our products, U.S. product candidate, technologies and business, including our implementation thereof;
• commercial success and market acceptance of our products and U.S. product candidate;
• our ability to achieve and maintain adequate levels of coverage or reimbursement for FemBloc or any future product candidates, and our products we seek to commercialize;
• our ability to accurately forecast customer demand for our products and U.S. product candidate, and manage our inventory;
• our ability to build, manage, and maintain our direct sales and marketing organization, and to market and sell our FemaSeed intratubal insemination product, FemBloc permanent birth control system, and women-specific medical product solutions in markets in and outside of the United States;
• our ability to establish, maintain, grow or increase sales and revenues;
• our expectations about market trends;
• our ability to continue operating as a going concern;
• the ability of our clinical trials to demonstrate safety and effectiveness of our U.S. product candidate, FemBloc, and other positive results;
• our ability to enroll subjects in the clinical trial for our U.S. product candidate, FemBloc, in order to advance the development thereof on a timely basis;
3
Table of Contents
• our ability to manufacture our products and U.S. product candidate, if approved, in compliance with applicable laws, regulations, and requirements and to oversee third-party suppliers, service providers and vendors in the performance of any contracted activities in accordance with applicable laws, regulations, and requirements;
• our ability to hire and retain our senior management and other highly qualified personnel;
• FDA or other U.S. or foreign regulatory actions affecting us or the healthcare industry generally, including healthcare reform measures in the United States and international markets;
• the timing or likelihood of regulatory filings and approvals or clearances;
• our ability to establish and maintain intellectual property protection for our products and U.S. product candidate and our ability to avoid claims of infringement; and
• the volatility of the trading price of our common stock.
The forward-looking statements in this Quarterly Report on Form 10-Q are only predictions and are based largely on our current expectations and projections about future events and financial trends that we believe may affect our business, financial condition and results of operations. These forward-looking statements speak only as of the date of this Quarterly Report on Form 10-Q and are subject to a number of known and unknown risks, uncertainties and assumptions, including those described under the sections in this Quarterly Report on Form 10-Q entitled “Risk Factors” and “Management's Discussion and Analysis of Financial Condition and Results of Operations” and elsewhere in this Quarterly Report on Form 10-Q. Because forward-looking statements are inherently subject to risks and uncertainties, some of which cannot be predicted or quantified and some of which are beyond our control, you should not rely on these forward-looking statements as predictions of future events. The events and circumstances reflected in our forward-looking statements may not be achieved or occur and actual results could differ materially from those projected in the forward-looking statements. Moreover, we operate in an evolving environment. New risk factors and uncertainties may emerge from time to time, and it is not possible for management to predict all risk factors and uncertainties. You should read this Quarterly Report on Form 10-Q and the documents that we reference in this Quarterly Report on Form 10-Q and have filed with the Securities and Exchange Commission (the “SEC”) as exhibits hereto completely and with the understanding that our actual future results may be materially different from any future results expressed or implied by these forward-looking statements. Except as required by applicable law, we do not plan to publicly update or revise any forward-looking statements contained herein, whether as a result of any new information, future events, changed circumstances or otherwise. The forward-looking statements contained in this Quarterly Report on Form 10-Q are excluded from the safe harbor protection provided by the Private Securities Litigation Reform Act of 1995 and Section 27A of the Securities Act of 1933, as amended.
4
Table of Contents
PART I. FINANCIAL INFORMATION
ITEM I.
Financial Statements
FEMASYS INC.
Condensed Balance Sheets
(unaudited)
Assets
March 31,
2026
December 31,
2025
Current assets:
Cash and cash equivalents
$
5,386,041
9,266,353
Accounts receivable, net
172,264
616,600
Inventory
6,105,267
5,740,249
Prepaid and other current assets
679,917
833,133
Total current assets
12,343,489
16,456,335
Property and equipment, at cost:
Leasehold improvements
1,238,886
1,238,886
Office equipment
80,941
78,155
Furniture and fixtures
421,798
417,876
Machinery and equipment
3,095,633
3,065,713
Construction in progress
955,271
897,885
5,792,529
5,698,515
Less accumulated depreciation
(
3,868,518
)
(
3,802,940
)
Net property and equipment
1,924,011
1,895,575
Long-term assets:
Lease right-of-use assets, net
1,178,941
1,297,121
Intangible assets, net of accumulated amortization
124,252
134,914
Other long-term assets
924,552
940,232
Total long-term assets
2,227,745
2,372,267
Total assets
$
16,495,245
20,724,177
(continued)
5
Table of Contents
FEMASYS INC.
Condensed Balance Sheets
(unaudited)
Liabilities and Stockholders’ Equity
March 31,
2026
December 31,
2025
Current liabilities:
Accounts payable
$
1,597,591
1,830,124
Accrued expenses
1,024,706
1,265,773
Clinical holdback – current portion
52,572
52,644
Operating lease liabilities – current portion
480,286
487,624
Total current liabilities
3,155,155
3,636,165
Long-term liabilities:
Clinical holdback – long-term portion
54,487
52,370
Convertible notes payable, net
3,335,176
3,178,864
Conversion option liability
488,000
2,014,000
Warrants liabilities
1,260,000
4,943,000
Operating lease liabilities – long-term portion
912,534
1,030,476
Total long-term liabilities
6,050,197
11,218,710
Total liabilities
9,205,352
14,854,875
Commitments and contingencies
Stockholders' equity:
Common stock, $
0.001
par,
200,000,000
authorized,
60,507,909
shares issued and
60,390,686
outstanding as of March 31, 2026; and
59,720,010
shares issued and
59,602,787
outstanding as of December 31, 2025
60,508
59,720
Treasury stock,
117,223
common shares
(
60,000
)
(
60,000
)
Warrants
5,246,150
5,246,150
Additional paid-in capital
147,023,279
146,449,576
Accumulated deficit
(
144,980,044
)
(
145,826,144
)
Total stockholders’ equity
7,289,893
5,869,302
Total liabilities and stockholders' equity
$
16,495,245
20,724,177
The accompanying notes are an integral part of these condensed unaudited financial statements.
6
Table of Contents
FEMASYS INC.
Condensed Statements of Comprehensive Income (Loss)
(unaudited)
Three Months Ended March 31,
2026
2025
Sales
$
424,889
341,264
Cost of sales (excluding depreciation expense)
158,606
117,266
Operating expenses:
Research and development
1,309,401
2,968,472
Sales and marketing
1,315,755
908,567
General and administrative
1,782,390
1,722,713
Depreciation and amortization
82,270
84,853
Total operating expenses
4,489,816
5,684,605
Loss from operations
(
4,223,533
)
(
5,460,607
)
Other income (expense):
Interest income
49,827
19,029
Change in fair value of conversion option liability
1,513,413
—
Change in fair value of warrants liabilities
3,683,000
—
Interest expense
(
176,607
)
(
459,449
)
Total other income (expense), net
5,069,633
(
440,420
)
Income (loss) before income taxes
846,100
(
5,901,027
)
Income tax benefit
—
(
4,188
)
Net income (loss)
$
846,100
(
5,896,839
)
Net income (loss) attributable to common stockholders
$
328,646
(
5,896,839
)
Earnings (losses) per share:
Basic earnings per share
$
0.00
(
0.23
)
Diluted earnings per share
$
0.00
(
0.23
)
Weighted average common shares outstanding:
Basic
66,645,591
25,149,236
Diluted
78,095,633
25,149,236
The accompanying notes are an integral part of these condensed unaudited financial statements.
7
Table of Contents
FEMASYS INC.
Condensed Statements of Stockholders’ Equity
(unaudited)
Common stock
Treasury common stock
Additional
Accumulated
Total
stockholders’
Shares
Amount
Shares
Amount
Warrants
paid-in capital
deficit
equity
THREE MONTHS ENDED MARCH 31, 2026
Balance at December 31, 2025
59,602,787
$
59,720
117,223
$
(
60,000
)
$
5,246,150
$
146,449,576
$
(
145,826,144
)
$
5,869,302
Issuance of common stock in connection with at-the-market offering, net of issuance costs
623,911
624
—
—
—
341,536
—
342,160
Issuance of common shares in payment of 2023 convertible note interest, including related parties
60,559
61
—
—
—
47,780
—
47,841
Conversion of 2025 convertible notes into common stock
103,429
103
—
—
—
32,779
—
32,882
Share-based compensation expense
—
—
—
—
—
151,608
—
151,608
Net income
—
—
—
—
—
—
846,100
846,100
Balance at March 31, 2026
60,390,686
$
60,508
117,223
$
(
60,000
)
$
5,246,150
$
147,023,279
$
(
144,980,044
)
$
7,289,893
THREE MONTHS ENDED MARCH 31, 2025
Balance at December 31, 2024
23,355,926
$
23,473
117,223
$
(
60,000
)
$
1,860,008
$
127,679,198
$
(
127,198,257
)
$
2,304,422
Issuance of common stock in connection with at-the-market offering, net of issuance costs
3,731,960
3,732
—
—
—
5,218,165
—
5,221,897
Share-based compensation expense
—
—
—
—
—
367,237
—
367,237
Net loss
—
—
—
—
—
—
(
5,896,839
)
(
5,896,839
)
Balance at March 31, 2025
27,087,886
$
27,205
117,223
$
(
60,000
)
$
1,860,008
$
133,264,600
$
(
133,095,096
)
$
1,996,717
The accompanying notes are an integral part of these condensed unaudited financial statements.
8
Table of Contents
FEMASYS INC.
Condensed Statements of Cash Flows
(unaudited)
Three Months Ended
March 31
2026
2025
Cash flows from operating activities:
Net income (loss)
$
846,100
(
5,896,839
)
Adjustments to reconcile net income (loss) to net cash used in operating activities:
Depreciation
65,578
77,682
Amortization
16,692
7,171
Change in fair value of conversion option liability
(
1,513,413
)
—
Change in fair value of warrants liabilities
(
3,683,000
)
—
Amortization of right-of-use assets
118,180
132,207
Loss on fixed asset dispositions
—
43,507
Share-based compensation expense
151,608
367,237
Amortization of debt issuance costs and discount
176,607
356,699
Changes in operating assets and liabilities:
Accounts receivable
444,336
254,775
Inventory
(
365,018
)
(
815,865
)
Prepaid and other assets
168,722
(
53,523
)
Accounts payable
(
253,439
)
890,678
Accrued expenses
(
193,226
)
19,239
Lease liabilities
(
125,280
)
(
133,076
)
Other liabilities
2,045
(
15,106
)
Net cash used in operating activities
(
4,143,508
)
(
4,765,214
)
Cash flows from investing activities:
Purchases of property and equipment
(
79,138
)
(
96,605
)
Net cash used in investing activities
(
79,138
)
(
96,605
)
Cash flows from financing activities:
Proceeds from at-the-market sales of common stock
352,922
5,392,027
Issuance costs for at-the-market sales of common stock
(
10,588
)
(
161,761
)
Net cash provided by financing activities
342,334
5,230,266
Net change in cash and cash equivalents
(
3,880,312
)
368,447
Cash and cash equivalents:
Beginning of period
9,266,353
3,451,761
End of period
$
5,386,041
3,820,208
Supplemental cash flow information
Cash paid for:
Interest
$
—
—
Income taxes
—
—
Non-cash investing and financing activities:
Property and equipment costs included in accounts payable
14,876
22,072
Acquisition of patents included in accounts payable
6,030
—
Conversion of November 2025 convertible notes into common stock
76,452
—
Payment of November 2023 convertible note interest in common stock
47,841
—
Deferred offering costs reclassified to additional paid-in capital
174
8,369
The accompanying notes are an integral part of these condensed unaudited financial statements.
9
Table of Contents
FEMASYS INC.
Condensed Notes to Financial Statements
(unaudited)
(1)
Organization, Nature of Business, and Liquidity
Organization and Nature of Business
Femasys Inc. (the “Company” or “Femasys”) was incorporated in Delaware on February 19, 2004 and is headquartered in Suwanee, Georgia. The Company is a leading biomedical innovator, addressing significant unmet needs in women's health worldwide, with a broad patent-protected portfolio of disruptive, accessible, in-office therapeutic and diagnostic products. The Company is a U.S. manufacturer that has received global regulatory approvals for its product portfolio, which are currently being commercialized in the U.S. and key international markets. The Company’s suite of products and U.S. product candidate address what the Company believes are multi-billion dollar global market segments in which there has been little advancement for many years, helping women avoid pharmaceutical solutions, implants and surgery that can be expensive and expose women to harm.
Basis of Presentation
The Company has prepared the accompanying condensed financial statements pursuant to the rules and regulations of the U.S. Securities and Exchange Commission (SEC). Certain information and footnote disclosures normally included in the annual financial statements prepared in accordance with accounting principles generally accepted in the United States of America (U.S. GAAP) have been condensed or omitted pursuant to these rules and regulations. These condensed financial statements should be read in conjunction with the Company’s audited financial statements and footnotes related thereto for the year ended December 31, 2025 included in our Annual Report on Form 10-K filed with the SEC on March 31, 2026 (the Annual Report). There have been no material changes to the Company’s significant accounting policies described in Note 2 to the financial statements included in the Annual Report.
10
Table of Contents
FEMASYS INC.
Condensed Notes to Financial Statements
(unaudited)
In the opinion of management, the unaudited condensed financial statements include all adjustments (consisting only of normal recurring adjustments) necessary to present fairly the Company’s financial position and the results of its operations and cash flows at the dates for the periods presented. The results of operations for such interim periods are not necessarily indicative of the results expected for the full year.
Use of Estimates
The preparation of financial statements in conformity with U.S. GAAP requires the Company to make estimates and assumptions that affect the reported amounts of assets and liabilities and disclosure of contingent assets and liabilities at the date of the financial statements, and the reported amounts of revenue and expense during the reporting periods. Estimates for these and other items are subject to change and are reassessed by management in accordance with U.S. GAAP. Actual results could differ from those estimates.
Liquidity
As of March 31, 2026, the Company had cash and cash equivalents of $
5,386,041
. The Company plans to finance its operations and commercial and development needs with its existing cash and cash equivalents, additional equity and/or debt financing arrangements, and revenue primarily anticipated from domestic sales of FemaSeed and FemVue and international sales of FemBloc, FemaSeed, and FemVue to support the Company’s commercial efforts and research and development activities, primarily focused on FemBloc. There can be no assurance that the Company will be able to obtain additional financing on terms acceptable to the Company, on a timely basis, or at all. If the Company is not able to obtain sufficient funds on acceptable terms when needed, the Company’s business, results of operations, and financial condition could be materially adversely impacted.
For the three months ended March 31, 2026, the Company generated net income of $
846,100
. The Company expects losses to increase over the next few years as the Company commercializes FemaSeed and its other products and advances FemBloc through clinical development if and until FDA approval is received and the product is available to be marketed in the U.S.
The financial statements have been prepared on a going-concern basis, which contemplates the realization of assets and the satisfaction of liabilities in the normal course of business. The Company has incurred net operating losses in every year since inception with the exception of the three months ended March 31, 2026. The Company has an accumulated deficit as of March 31, 2026 of $
144,980,044
and expects to incur additional losses and negative operating cash flows for at least the next twelve months. The Company’s ability to meet its obligations is dependent upon its ability to generate sufficient cash flows from operations and future financing transactions. Although management expects the Company will continue as a going concern, there is no assurance that management’s plans will be successful because the availability and amount of such funding are not certain. Accordingly, substantial doubt exists about the Company’s ability to continue as a going concern for at least one year from the issuance of these financial statements. The accompanying financial statements do not include any adjustments to reflect the possible future effects on the recoverability of assets or the amounts and classifications of liabilities that may result from the possible inability of the Company to continue as a going concern.
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FEMASYS INC.
Condensed Notes to Financial Statements
(unaudited)
Recently Issued Accounting Pronouncements
–
Recently Adopted
In November 2024, the FASB issued ASU 2024-04,
Debt—Debt with Conversion and Other Options (Subtopic 470-20): Induced Conversions of Convertible Debt Instruments
. The ASU clarifies the accounting for induced conversion of convertible debt instruments and requires entities to recognize the fair value of any incremental consideration provided to induce conversion as expense. ASU 2024-04 is effective for the Company’s annual reporting periods beginning after December 15, 2025. The Company adopted the ASU on January 1, 2026, and it did not have an impact on the Company’s financial statements.
Recently Issued Accounting Pronouncements – Not Yet Adopted
In November 2024, the FASB issued ASU 2024-03,
Disaggregation of Income Statement Expenses (Subtopic 220-40)
. The standard requires public business entities to disclose additional information about specific expense categories included in relevant income statement captions, including purchases of inventory, employee compensation, depreciation, amortization of intangible assets, and certain other expenses. ASU 2024-03 is effective for the Company’s annual reporting periods beginning after December 15, 2026. Early adoption is permitted. The ASU may be applied either with a prospective or a fully retrospective transition method. Management is currently assessing the impact of this standard on the Company’s financial statements and will adopt the ASU on January 1, 2027.
In December 2025, the FASB issued ASU 2025-11,
Interim Reporting (Topic 270): Narrow-Scope Improvements
. The amendments clarify the applicability of the interim reporting guidance in Topic 270 and improve the navigability of interim disclosure requirements by providing a more comprehensive listing of disclosures required in interim financial statements. The ASU is effective for the Company’s interim periods in annual reporting periods beginning after December 15, 2027. Early adoption is permitted. The ASU may be applied either with a prospective method or a fully retrospective method of transition. Management is currently assessing the impact of this standard on the Company’s financial statements and will adopt the ASU on January 1, 2028.
No other new accounting pronouncements issued or effective have had, or are expected to have, a material impact on the Company’s financial statements.
(2)
Fair Value of Financial Instruments
The Company applies a fair value hierarchy that requires the use of observable market data, when available, and prioritizes the inputs to valuation techniques used to measure fair value in the following categories:
Level 1 – Valuation is based upon quoted prices for identical instruments traded in active markets.
Level 2 – Valuation is based upon quoted prices for similar instruments in active markets, quoted prices for identical or similar instruments in markets that are not active, and model‑based valuation techniques for which all significant assumptions are observable in the market.
Level 3 – Valuation is generated from model‑based techniques that use significant assumptions not observable in the market. These unobservable assumptions reflect the Company’s own estimates of assumptions market participants would use in pricing the asset or liability.
Certain of the Company’s financial instruments, including cash and cash equivalents, accounts receivable and other liabilities approximate their fair value because of the short‑term maturity of these financial instruments.
12
Table of Contents
The following fair value hierarchy table presents information about the Company’s assets and liabilities measured at fair value on a recurring basis:
Fair value measurement at
Reporting Date
(Level 1)
(Level 2)
(Level 3)
As of March 31, 2026
Liabilities:
AMPA liability
$
-
Conversion Option liability
$
488,000
Warrants liabilities
$
1,260,000
The fair value of the AMPA (see Note 9) was measured before and after the March 19, 2026 modification and as of the March 31, 2026 reporting period using Level 3 inputs. The fair value was deemed de minimis at both date of issuance date and as of the March 31, 2026 reporting period.
The fair value of the Conversion Option liability and Warrants liabilities related to the 2025 Notes (see Note 8b) were measured
as of December 31, 2025 and as of the
March 31, 2026 reporting period. The change in fair value between the periods was recognized as gains in other income
(expense)
in the statements of comprehensive income (loss).
The Company also recognized a change in fair value as a result of the modification of the Conversion Option and Warrants on March 19, 2026 which was offset by the issuance of the Series D-1 Warrants as discussed further below.
Activity during the quarter ended March 31, 2026 is summarized below:
Fair Value of
Conversion Option
Liability
Fair Value of Warrants Liabilities
Balance at December 31, 2025
$
2,014,000
$
4,943,000
Change in fair value other than modification
(
1,112,413
)
(
4,084,000
)
Change in fair value related to March 19, 2026 modification
(
401,000
)
(
1,801,000
)
Issuance of Series D-1 Warrants
—
2,202,000
Conversion of convertible note
(
12,587
)
—
Balance at March 31, 2026
$
488,000
$
1,260,000
The March 31, 2026 fair value of the Conversion Option liability and Warrants liabilities were estimated using the Black-Scholes option pricing model Level 3 inputs, with the following assumptions:
Conversion
Option
Liability
Warrants
Liabilities
Expected term (in years)
2.59
2.59
Risk‑free interest rate
3.7
%
3.7
%
Dividend yield
—
%
—
%
Expected volatility
30
%
30
%
Exercise price
$
0.73
$
0.58
-
1.10
Stock price
$
0.42
$
0.42
Black-Scholes value
$
0.023
$
0.004
-
0.047
The valuations of the Conversion Option liability and Warrants liabilities at modification in Q1 2026 (see Note 8b) were calibrated such that the aggregate change in fair values of the outstanding Conversion Option and Warrants equaled the fair value of the Series D-1 Warrants issued on the modification date. This calibration resulted in an expected volatility assumption of
30
%, which was also the volatility assumption used to value the Conversion Option liability and Warrants liabilities as of March 31, 2026. If the Company used the historical volatility of its common stock as the expected volatility assumption, the estimated value of the Conversion Option liability and Warrants liabilities would be higher. The expected terms of the Conversion Option and Warrants as of March 31, 2026, were consistent with the terms used as of December 31, 2025, which were based on the Company’s option to mandate conversion of the Notes upon achieving certain milestones (see Note 8b) as well as the expectation that the Warrants will be exercised upon a significant increase in the price of the Company’s common stock. If the Company used the contractual term of the Conversion Option and Warrants as the expected term, the estimated value of the Conversion Option liability and Warrants liabilities would be higher.
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Table of Contents
We review the fair value hierarchy classification of our applicable assets and liabilities on a quarterly basis. Changes in the observability of valuation inputs may result in a reclassification for certain financial assets or liabilities. During the quarter ended March 31, 2026, there were no transfers between Level 1, Level 2 and Level 3.
The carrying amounts of cash and cash equivalents, accounts receivable, customer deposits, accounts payable and accrued expenses approximate fair value due to their short-term nature. As of March 31, 2026, the fair value of the 2025 notes (excluding the conversion option, see Note 8b), calculated using a discounted cash flow analysis using Level 3 inputs, was approximately $
3.8
million. The Company uses a Black-Scholes option valuation model to determine the grant date fair value of employee stock options which uses Level 2 inputs. See Note 10 for a description of inputs used.
(3)
Cash and Cash Equivalents
As of March 31, 2026 and December 31, 2025, money market funds and short-term U.S. Treasury bills included in cash and cash equivalents on the balance sheets were $
4,156,792
and $
7,110,655
, respectively, which represent Level 1 within the fair value hierarchy. The Company considers all highly liquid investments with an initial maturity of three months or less when purchased to be cash equivalents.
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Table of Contents
FEMASYS INC.
Condensed Notes to Financial Statements
(unaudited)
(4)
Inventories
Inventory, stated at cost, consisted of the following:
March 31,
December 31,
2026
2025
Materials
$
2,048,291
2,060,521
Work in progress
1,584,374
1,266,542
Finished goods
2,472,602
2,413,186
Inventory
$
6,105,267
5,740,249
(5)
Accrued Expenses
Accrued expenses included the following:
March 31,
December 31,
2026
2025
Incentive and other compensation costs
$
753,161
870,910
Clinical trial costs
170,459
259,293
Director fees
71,250
71,250
Other
29,836
64,320
Accrued expenses
$
1,024,706
1,265,773
(6)
Revenue Recognition
Revenue is recognized upon shipment of our goods based upon contractually stated pricing at standard payment terms typically ranging from
30
to
60
days. All revenue is recognized at a point in time. As of March 31, 2026, there were
no
unsatisfied performance obligations.
The majority of products sold directly to U.S. customers are shipped via common carrier, and the customer pays for shipping and handling and assumes control Free on Board (FOB) shipping point. Products shipped to our international distributors are in accordance with their respective agreements; however, the shipping terms are generally EX-Works, reflecting that control is assumed by the distributor at the shipping point. Returns are only accepted with prior authorization from the Company. Items to be returned must be in original unopened cartons and are subject to a
30
% restocking fee. Throughout the periods presented, the Company has not had a history of significant returns.
The following table summarizes our sales by geographic region:
Three Months Ended
March 31,
Primary geographical markets
2026
2025
U.S.
$
367,331
341,264
International
57,558
—
Total
$
424,889
341,264
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Table of Contents
FEMASYS INC.
Condensed Notes to Financial Statements
(unaudited)
(7)
Commitments and Contingencies
Legal Claims
Occasionally, the Company may be a party to legal claims or proceedings, the outcomes of which are subject to significant uncertainty. In accordance with Accounting Standards Codification (ASC) 450,
Contingencies
, the Company will assess the likelihood of an adverse judgment for any outstanding claim as well as ranges of probable losses. When it has been determined that a loss is probable and the amount can be reasonably estimated, the Company will record a liability. For both periods presented, there were no material legal contingencies requiring accrual or disclosure.
The Company, as permitted under Delaware law and in accordance with its bylaws, indemnifies its officers and directors for certain events or occurrences, subject to certain limits, while the officer or director is or was serving at the Company’s request in such capacity. The Company entered into employment agreements with its officers, which provide for indemnification protection in the executive’s capacity as an officer for actions taken within the scope of employment. The maximum amount of potential future indemnification is unlimited; however, the Company has obtained director and officer insurance that limits its exposure. The Company believes the fair value for these indemnification obligations is minimal. Accordingly, the Company has not recognized any liabilities relating to these obligations as of March 31, 2026 and December 31, 2025.
(8)
Convertible Notes with Warrants
(a)
Convertible Notes with Warrants (November 2023 Financing)
On November 21, 2023, the Company issued (i) senior unsecured convertible notes (“Notes”) in an aggregate principal amount of $
6,850,000
, (“2023 Notes”), convertible into shares of common stock at a conversion price of $
1.18
per share, (ii) Series A Warrants to purchase up to an aggregate of
5,805,083
shares of common stock at an exercise price of $
1.18
per share, and (iii) Series B Warrants, together with the Series A Warrants, and, together with the convertible notes, to purchase up to an aggregate of
5,805,083
shares of common stock at an exercise price of $
1.475
per share. The financing resulted in aggregate gross proceeds of $
6,850,000
, before $
525,144
of issuance costs.
The 2023 Notes accrued interest at a rate of
6.0
% per annum, payable annually, in cash or shares of common stock at the Company’s option. In November 2024, the Company paid $
111,000
of accrued interest in cash and $
300,000
accrued interest in
315,790
shares of common stock. In November 2025, the Company paid $
407,841
in accrued interest in
516,256
shares of common stock.
As noted above, the 2023 Notes were convertible into shares of common stock at the election of the holder at any time at an initial conversion price of $
1.18
. The conversion feature did not meet the requirements for separate accounting and was not accounted for as a derivative instrument. In April 2025, $
85,000
of convertible notes were converted into
72,033
shares of common stock. The 2023 Notes matured on
November 21, 2025
, and were repaid in full by the Company with proceeds from the November 2025 Financing discussed below.
No
gain or loss was recorded upon repayment of the 2023 Notes.
Warrants
The Series A Warrants are exercisable immediately and expire
five years
from the date of issuance. The Company has the right to call the exercise of the Series A Warrants if the closing price of the common stock exceeds
200
% of the Series A Exercise Price for
10
consecutive trading days and the daily dollar trading volume of the common stock exceeds $
1,000,000
per day during the same period and certain equity conditions are satisfied.
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Table of Contents
FEMASYS INC.
Condensed Notes to Financial Statements
(unaudited)
The Series B Warrants expired in
November 2024
.
The Series A Warrants are classified as a component of permanent equity because they are freestanding financial instruments that are legally detachable and separately exercisable from the shares of common stock from which they are issued, are immediately exercisable, do not embody an obligation for the Company to repurchase its shares, and permit the holders to receive a fixed number of shares of common stock upon exercise.
For the three months ended March 31, 2025, the Company recognized total interest expense on the 2023 Notes of $
459,449
, including coupon interest expense of $
102,750
and amortization of debt discount and issuance costs of $
356,699
.
(b)
Convertible Notes with Warrants (November 2025 Financing)
In November 2025, the Company issued (i) senior secured convertible notes (“2025 Notes”) in an aggregate principal amount of $
12,000,000
, convertible into
16,378,563
shares of common stock at a conversion price of $
0.73
per share, (ii) Series A-1 Warrants to purchase up to an aggregate of
16,378,563
shares of common stock at an exercise price of $
0.81
per share, subject to adjustments, (iii) Series B-1 Warrants to purchase an aggregate of
16,378,563
shares of common stock at an exercise price of $
0.92
per share, subject to adjustments, and (iv) Series C-1 Warrants to purchase an aggregate of
16,378,563
shares of common stock at an exercise price of $
1.10
per share, subject to adjustments (Series A-1 Warrants, Series B-1 Warrants and Series C-1 Warrants are collectively the “Warrants”). The financing resulted in aggregate gross proceeds of $
12,000,000
, before $
718,528
of issuance costs.
The 2025 Notes accrue interest at a rate of
8.5
% per annum, payable
annually
in-kind by increasing the principal balance outstanding. The Company granted a security interest in substantially all of its assets to the holders of the 2025 Notes. The 2025 Notes mature in
November 2035
. The Company has a call option where it may voluntarily redeem the 2025 Notes after
seven and one half years
from Note issuance at
112
% of the then-outstanding principal.
The 2025 Notes are convertible into shares of common stock at the election of the holder at any time (“Conversion Option”) at an initial conversion price of $
0.73
(“Conversion Price”). The Conversion Price is adjustable proportionally for certain events including stock splits, reverse stock splits and stock dividends (each a “Share Combination Event”). Additionally, prior to the March 2026 modification discussed below, upon a Share Combination Event, the conversion price would also have been further adjusted to the lowest dollar volume-weighted average price (VWAP) of the Company’s common stock during the five-day period following any Share Combination Event, but only if the conversion price (after the standard proportional adjustment) was higher than the market price.
The Company may require conversion of the 2025 Notes, in whole or in part, if at any time (i) a Registration Statement is effective, (ii) for the immediately preceding thirty (
30
) consecutive trading days, the VWAP has exceeded
450
% of the then-effective Conversion Price on each such trading day, (iii) the total daily trading volume of the Common Stock is at least $
1,500,000
, and (iv) certain equity conditions are satisfied (effective registration statement is available and sufficient authorized shares are available, among other conditions). The holders of the 2025 Notes may require prepayment of principal and accrued interest upon certain Events of Default (failure to timely pay amounts owed under the 2025 Notes, failure to deliver shares upon conversion of the 2025 Notes or exercise of the related Warrants, failure to maintain an effective registration statement related to the common shares underlying the 2025 Notes and related Warrants, etc.), and the Company must redeem the 2025 Notes if involuntary bankruptcy proceedings are initiated against the Company and not dismissed within
60
days or if the Company voluntarily initiates bankruptcy. Additionally, in the event of certain merger, acquisition or business combination transactions (a "Fundamental Transaction" as defined in the 2025 Notes), the Company must redeem the 2025 Notes, and if the Fundamental Transaction occurs in the first
5
years of note issuance, the redemption will include a premium.
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Table of Contents
If the Company offers future rights such as convertible securities, options, or warrants to purchase common stock to common stockholders (“Purchase Rights”), the holder of the 2025 Notes are likewise entitled to receive such Purchase Rights as if the Notes were converted and the corresponding shares of common stock were outstanding.
As of March 31, 2026, $
76,452
of the 2025 Notes and accrued interest thereon were converted into
103,429
shares of common stock.
Warrants
The Series A-1 Warrants are exercisable immediately and expire
ten years
from the date of issuance. The Series B-1 Warrants are exercisable immediately and expire at the earlier of (i) the
tenth
anniversary of the issuance of the Warrants, or (ii)
45
days after the Company discloses
two
consecutive quarters of at least $
3.25
million in sales. The Series C-1 Warrants are exercisable immediately and expire at the earlier of (i) the
tenth
anniversary of the issuance of the Warrants, or (ii)
45
days after the Company discloses FDA approval of FemBloc.
The exercise price of the Warrants and the related number of shares into which the Warrants are exercisable are adjustable proportionally in the event of a Share Combination Event. Additionally, similar to the Conversion Option in the 2025 Notes and prior to the March 2026 modification discussed below, upon a Share Combination Event, the exercise prices of the Warrants would also have been further adjusted to the lowest VWAP of the Company’s common stock during the
five-day
period following any Share Combination Event, but only if the exercise price (after the standard proportional adjustment) was higher than the market price.
In the event of a Fundamental Transaction within the Company’s control, the holders of the Warrants are entitled to put the unexercised portion of the Warrants to the Company in exchange for cash at their then Black-Scholes value. If the Fundamental Transaction is outside of the Company’s control, the holders of the Warrants may receive consideration for the unexercised portion of the Warrants equal to the then Black-Scholes value in the same form (cash or equity) as other common shareholders pursuant to the Fundamental Transaction.
If the Company offers future rights such as convertible securities, options, or warrants to purchase common stock to common stockholders (“Purchase Rights”), the holders of the Warrants are likewise entitled to receive such Purchase Rights as if the Warrants were exercised and the corresponding shares of common stock were outstanding.
As of March 31, 2026,
no
Warrants have been exercised.
In March 2026, the Company modified the Conversion Option in the 2025 Notes and related Warrants to remove the market-related adjustment to the conversion price and exercise prices, respectively, that would have occurred upon a Share Combination Event. As consideration for this modification, the Company issued the holders of the 2025 Notes and related Warrants new Series D-1 Warrants which allow the holders to purchase an aggregate number of
16,378,563
shares of the Company’s common stock. The exercise price of the Series D-1 Warrants is $
0.58
per share, and the Series D-1 Warrants expire in March 2029.
The 2025 Notes and Warrants (including the new Series D-1 Warrants) are freestanding financial instruments that are legally detachable and separately exercisable. Due to the adjustments to the conversion price of the 2025 Notes and the exercise prices of the Warrants upon a Share Combination Event beyond a standard proportional adjustment (but only if the market price of the Company’s common stock is lower than the Conversion Price of the 2025 Notes or exercise prices of the Warrants) and due to the requirement that shareholder approval be obtained for conversion and exercises that would exceed
19.99
% of the outstanding shares of the Company, both the Conversion Option and the Warrants (including the new Series D-1 Warrants) were determined to be not indexed to the Company’s common stock. As a result, at issuance, the Conversion Option was bifurcated from the 2025 Notes, and both the Conversion Option and Warrants were recognized as derivative liabilities on the Company’s balance sheet. Likewise, the Series D-1 Warrants were recognized as derivative liabilities on the Company’s balance sheet upon issuance in March 2026. The Conversion Option and Warrants (including the Series D-1 Warrants) will be remeasured at fair value every reporting period. The Notes are accreted to their maturity value based on the effective interest method. For the three months ended March 31, 2026, the Company recognized total interest expense on the 2025 Notes of $
176,607
related to the amortization of debt discount and issuance costs. The effective interest rate of the 2025 Notes is approximately
21.9
%.
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Table of Contents
See Note 2 for further detail regarding fair value of the 2025 Notes, Conversion Option and Warrants liabilities.
The following summarizes the carrying values of the 2025 Notes as of March 31, 2026 and December 31, 2025:
Stated
Interest
Rate
March 31,
2026
December 31,
2025
Face value of November 2025 Notes
8.5
%
11,925,000
12,000,000
PIK interest on November 2025 Notes
384,660
132,139
Less unamortized discount and debt issuance costs
(
8,974,484
)
(
8,953,275
)
Convertible Notes Payable
$
3,335,176
$
3,178,864
No amounts are due under the 2025 Notes until they mature in November 2035.
(9)
Stockholders’ Equity
On July 1, 2022, the Company filed a shelf registration statement to sell up to $
150
million in common and preferred stock, debt securities and warrants. Additionally, the Company entered into an Equity Distribution Agreement with Piper Sandler & Co. (the “Sales Agent”) and filed a related prospectus establishing an “at-the-market” facility, pursuant to which the Company may offer and sell shares of common stock from time to time through the Sales Agent. In October 2023, the Sales Agent was authorized to sell shares for aggregate proceeds up to $
16.7
million at current market prices until all shares are sold.
For the three months ended March 31, 2026, the Company sold approximately
624,000
shares of common stock for aggregate proceeds of approximately $
353
,000, and as of March 31, 2026, approximately $
9.4
million remained available for sale pursuant to the prospectus. As of March 31, 2026, the amount the Company was authorized to sell was subject to baby-shelf limitations.
Under SEC Rule 415(a)(1)(x), companies whose public float is less than $75 million are limited in the aggregate amount of securities that may be sold on a primary basis under a shelf registration statement during any twelve-month period to no more than one-third of such company's public float. As of March 31, 2026, the Company’s public float was below $75 million, and the one-third limit constrains the total amount of common stock it is able to sell under the Equity Distribution Agreement in any twelve-month period to an amount that may be substantially less than the approximately $9.5 million of capacity nominally available under the prospectus.
June 2025 Financing
In June 2025, the Company sold
3,600,000
shares of common stock in an underwritten public offering at $
0.85
per share. The Company also sold
1,686,275
shares of common stock in a separate concurrent private placement at a price of $
0.85
per share to certain existing institutional stockholders and a price of $
1.02
per share to certain directors and officers. The offering resulted in aggregate gross proceeds of $
4,510,001
, before $
804,940
of transaction costs.
Additionally, common warrants to purchase
105,726
shares of common stock were issued to the underwriter as a commission for services performed. The underwriter warrants are exercisable beginning December 2, 2025, have a
5
-year term and an exercise price of $
1.0625
per share. The warrants are classified as a component of permanent equity because they are freestanding financial instruments that are legally detachable and separately exercisable from the shares of common stock from which they are issued, do not embody an obligation for the Company to repurchase its shares, and permit the holders to receive a fixed number of shares of common stock upon exercise. The warrants were valued at $
56,035
using Black-Scholes assumptions. As of March 31, 2026,
105,726
underwriter warrants remain outstanding.
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Table of Contents
Any Market Purchase Agreement (“AMPA”)
On June 30, 2025, the Company entered into an Any Market Purchase Agreement (“Purchase Agreement” or “AMPA”) with Alumni Capital LP (“Alumni”) whereby the Company has the right, but not obligation, to sell to Alumni up to an aggregate of $
10
million in shares of common stock in a series of purchases until December 31, 2026. The Company may elect that Alumni purchase up to $
1
million in shares of common stock (or up to $
5
million if mutually agreed) at either (i) the lowest traded price for the
four
previous business
days
, multiplied by
90
% or (ii) up to the lesser of (a) $
1
million in shares of common stock or (b)
100
% of the average daily trading volume of common stock for the previous
two
business
days
at lowest daily dollar volume-weighted average price, multiplied by
97
%. The Company is limited to issuances to Alumni of up to
19.99
% of the shares of common stock outstanding immediately prior to the execution of the Purchase Agreement. The Purchase Agreement allows the Company to raise equity on a periodic basis at its discretion depending on a variety of factors including market conditions, the trading price of the common stock, and use of proceeds for operating activities. Due to certain pricing and settlement provisions, the Purchase Agreement includes an embedded put option contract. The Company accounts for the Purchase Agreement as a derivative, with a fair value deemed de minimis. The difference between the discounted purchase price and the fair value of the shares is expensed in the period the transaction occurs as a non-cash, non-operating financing cost. See Note 2 for further detail regarding fair value of the AMPA.
As of March 31, 2026,
no
shares have been sold under the AMPA.
August 2025 Financing
On August 25, 2025, the Company entered into a securities purchase agreement pursuant to which the Company sold (i)
10,434,586
shares of common stock in a public offering and to certain Company officers, (ii) pre-funded warrants to purchase
11,750,000
shares of common stock, and (iii) common warrants to purchase
22,184,586
shares of common stock. Additionally, common warrants to purchase
443,692
shares of common stock were issued to the underwriter as compensation for services performed.
The pre-funded warrants, common warrants and underwriter warrants were exercisable immediately following the closing date of the offering. The pre-funded warrants have an unlimited term and an exercise price of $
0.0001
per share. The common warrants have a
5
-year term and an exercise price of $
0.36
per share, except for common warrants sold to certain Company officers, which have an exercise price of $
0.5151
per share. The underwriter warrants have a
5
-year term and an exercise price of $
0.45
per share. The offering resulted in aggregate gross proceeds of $
7,998,826
, before $
930,132
of transaction costs.
The pre-funded warrants and common warrants are classified as a component of permanent equity because they are freestanding financial instruments that are legally detachable and separately exercisable from the shares of common stock with which they were issued, are immediately exercisable, do not embody an obligation for the Company to repurchase its shares, and permit the holders to receive a fixed number of shares of common stock upon exercise.
The common stock was valued at $
3,770,001
, based on the Company’s stock price. The pre-funded warrants and common warrants were valued at $
4,230,000
and $
5,324,301
, respectively, using the following Black-Scholes assumptions:
Pre-funded warrants
Common warrants
Underwriter warrants
Expected term (in years)
4
4
4
Risk‑free interest rate
3.64
%
3.64
%
3.64
%
Dividend yield
—
%
—
%
—
%
Expected volatility
90.63
%
90.63
%
90.63
%
Exercise price
$
0.0001
$
0.36
- $
0.5151
$
0.45
Stock price
$
0.36
$
0.36
- $
0.5151
$
0.36
Black-Scholes value
$
0.36
$
0.24
-
0.27
$
0.22
The net proceeds of $
7,068,694
were allocated to the common stock, pre-funded warrants and common warrants using the relative fair value method and were recorded to stockholders’ equity.
As of March 31, 2026,
6,750,000
pre-funded warrants,
12,965,476
common warrants and
443,692
placement agent warrants remain outstanding.
20
Table of Contents
FEMASYS INC.
Condensed Notes to Financial Statements
(unaudited)
(10)
Equity Incentive Plans and Warrants
In June 2021, in connection with the IPO, the 2021 Equity Incentive Plan (2021 Plan) became effective, which was adopted by the Board of Directors in February 2021 and approved by stockholders in March 2021. As of March 31, 2026, approximately
5,233,948
shares were reserved for future issuance under the Company’s stock plans for stock options and RSUs.
Stock-Based Awards
(a)
Stock Option Plans
Activity under the Company’s stock option plans for the three months ended March 31, 2026 was as follows:
Number
of
options
Weighted
average
exercise
price
Aggregate
Intrinsic
Value
Outstanding at December 31, 2025
3,830,391
$
1.47
92,127
Granted
45,200
0.60
Forfeited
(
623,322
)
1.36
Outstanding at March 31, 2026
3,252,269
$
1.48
$
—
Vested and exercisable at March 31, 2026
1,904,941
$
1.85
$
—
The intrinsic value represents the amount by which the market price of the underlying stock at March 31, 2026 exceeds the exercise price of an option.
(b)
Inducement Grants
Since 2023, the Company has granted inducement grants, a stock option grant to certain employees for the right to purchase shares, which were approved by the Compensation Committee. The inducement grants vest in equal installments over
four years
provided the employee remains employed by the Company on the vesting date. In the first quarter of 2026,
335,000
options were granted and
37,500
options were forfeited.
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FEMASYS INC.
Condensed Notes to Financial Statements
(unaudited)
The inducement grants are summarized as follows:
Number
of
options
Weighted
average
exercise
price
Weighted
average
remaining
life years
Outstanding at December 31, 2025
137,500
$
2.52
4.53
Granted
335,000
0.46
9.94
Forfeited
(
37,500
)
1.32
—
Outstanding at March 31, 2026
435,000
$
1.04
9.02
Vested and exercisable at March 31, 2026
100,000
$
2.97
5.91
The Black-Scholes weighted- average assumptions for stock option awards granted in the first quarter of 2026 was as follows:
Three Months Ended
March 31, 2026
2021
Plan
Inducement
Grants
Fair Value of Awards
$
0.47
0.37
Grant Price
$
0.6
0.46
Expected term (in years)
6.06
6.25
Risk‑free interest rate
3.89
%
3.83
%
Dividend yield
—
%
—
%
Expected volatility
95.8
%
96.84
%
No
options were exercised for the three months ended March 31, 2026 under our stock option plans.
(c)
Restricted Stock Units (RSUs)
Restricted stock units were granted to employees in the first quarter of 2026 with service-based vesting conditions. Related activity during the three months ended March 31, 2026 was as follows:
Number
of
RSUs
Weighted
average
grant
date
fair value
Outstanding at December 31, 2025
—
$
—
Granted
1,435,000
0.54
Forfeited
(
5,000
)
0.52
Outstanding at March 31, 2026
1,430,000
$
0.54
22
Table of Contents
(d)
Share-Based Compensation Expense
The following table shows the share-based compensation expense related to vested stock option and RSU grants to employees and nonemployees by financial statement line item on the accompanying condensed statements of comprehensive loss:
Three Months Ended March 31,
2026
2025
Research and development
$
28,937
136,924
Sales and marketing
15,924
(
10,431
)
General and administrative
106,747
240,744
Total share-based compensation expense
$
151,608
367,237
Stock-based compensation expense by award type during the three months ended March 31, 2026 and 2025 was as follows:
Three Months Ended March 31,
2026
2025
Stock options
$
106,875
367,237
Restricted stock units
44,733
—
Total share-based compensation expense
$
151,608
367,237
As of March 31, 2026, the remaining share-based compensation expense for stock options that are expected to be recognized in future periods for employees and nonemployees is $
980,179
, over a weighted average period of
2.6
years.
As of March 31, 2026, the remaining share-based compensation expense for RSUs that is expected to be recognized in future periods for employees is $
730,997
, over a weighted average period of
3.0
years.
(e)
Employee Stock Purchase Plan (ESPP)
For the three months ended March 31, 2026,
no
shares of common stock were issued under the Company’s ESPP Plan. As of March 31, 2026, the total number of shares of common stock reserved for future awards under the ESPP was
1,214,760
.
(11) Related‑Party Transactions
In November 2023, the Company issued unsecured convertible notes and accompanying Series A and Series B Warrants (see Note 8a). The transaction included the issuance of a $
5
million convertible note and
4,237,288
Series A and
4,237,288
Series B Warrants to PharmaCyte Biotech, Inc (“PharmaCyte”). The interim CEO, President and Director of PharmaCyte Biotech, Inc., Joshua Silverman, served on the Company’s board of directors until March 2026. The Series B Warrants expired in
November 2024
. In November 2025, the Company paid PharmaCyte accrued interest on the convertible note of $
300,000
in equity of
379,747
common shares. In November 2025, the convertible notes principal balance of $
5
million was repaid at maturity.
No
amounts were due to PharmaCyte as of March 31, 2026.
23
Table of Contents
In conjunction with the June 2025 Financing (see Note 9), certain executive officers and a director of the Company purchased an aggregate of
98,040
shares of the Company’s common stock in a private placement at a price of $
1.02
per share, for total gross proceeds of $
100,001
. Other investors in the private placement purchased common stock at a discounted price of $
0.85
per share.
No
amounts were due to or from these related parties in connection with this transaction as of March 31, 2026.
In conjunction with the August 2025 Financing (see Note 9), certain executive officers of the Company purchased
87,363
common shares, with a common warrant, with a combined price of $
0.5151
. Gross proceeds from the transaction totaled $
45,001
. The price equaled the market price of the Company’s stock on the applicable purchase date. The common warrants have a
5
-year term and an exercise price of $
0.5151
per share. The warrants remain outstanding as of March 31, 2026.
No
amounts were due to or from these related parties in connection with this transaction as of March 31, 2026.
In the November 2025 Financing (see Note 8b), certain executive officers and directors of the Company purchased senior secured convertible notes with a combined principal balance of $
175,000
, convertible into common shares at a price of $
0.73
per share. Additionally, in connection with the convertible notes, the officers and directors were issued
238,854
Series A-1 Warrants,
238,854
Series B-1 Warrants and
238,854
Series C-1 Warrants at exercise prices of $
0.81
, $
0.92
and $
1.10
per share, respectively. In March 2026, in connection with the modification of the Conversion Option in the 2025 Notes and the Series A-1, B-1, and C-1 Warrants, the officers and directors were issued
238,854
Series D-1 Warrants at exercise prices of $
0.58
per share. As of March 31, 2026, $
175,000
in convertible notes were due to the officers and directors, in addition to accrued interest of $
5,909
. All Series A-1,
Series
B-1,
Series
C-1 and
Series
D-1 warrants issued to the officers and directors remain outstanding as of March 31, 2026.
During the three months ended March 31, 2026 and year ended December 31, 2025, a family member of the CEO was employed by the Company. The compensation paid is consistent with market standards for comparable positions.
24
Table of Contents
FEMASYS INC.
Condensed Notes to Financial Statements
(unaudited)
(12)
Net Income (Loss) per Share Attributable to Common Stockholders
The Company presents basic and diluted earnings per share (“EPS”) data for its common stock. Basic EPS is calculated by dividing the income (loss) attributable to common stockholders by the weighted average number of shares of common stock outstanding during the period. Diluted EPS is determined by adjusting the net income (loss) attributable to common stockholders and the weighted-average number of shares of outstanding for the effects of potentially dilutive common shares, including stock options, restricted stock units, warrants and convertible notes, as applicable. Since the shares underlying the November 2025 pre-funded warrants were issuable for little consideration of $
0.0001
per share, they were considered outstanding for both basic and diluted loss per share from the date of issuance.
The Convertible Notes and certain warrants are considered participating securities under ASC 260
Earnings per Share,
because they entitle holders to participate in dividends on a nonforfeitable basis. Other warrants and the Company’s stock options and restricted stock units do not have such rights and are not considered participating securities.
When participating securities are present, ASC 260 requires the use of the two-class method when computing basic EPS. The two-class method is an earnings allocation formula that allocates net income to common stockholders and participating securities based on their respective rights to receive dividends and share in undistributed earnings. Participating securities do not have a contractual obligation to share in losses; therefore, net losses are not allocated to participating securities.
For diluted EPS, the Company evaluates the potential dilutive effect of participating securities and other instruments. Stock options, restricted stock units and certain warrants are included in diluted EPS using the treasury stock method, while convertible notes are evaluated using the if-converted method, if dilutive.
The following table sets forth the computation of the basic and diluted net income and (loss) per share:
Three Months Ended March 31,
2026
2025
BASIC EPS:
Net income (loss)
846,100
(
5,896,839
)
Less: Net (income) loss attributable to participating securities
(
517,454
)
—
Net income (loss) attributable to common stockholders
$
328,646
(
5,896,839
)
Weighted-average shares outstanding- Basic
66,645,591
25,149,236
Earnings (loss) per share- Basic
$
0.00
(
0.23
)
DILUTED EPS:
Net income (loss) attributable to common stockholders
$
328,646
(
5,896,839
)
Weighted-average shares outstanding- Basic
66,645,591
25,149,236
Add: Dilutive potential common shares
11,450,042
—
Weighted-average shares outstanding- Diluted
78,095,633
25,149,236
Earnings (loss) per share- Diluted
$
0.00
(
0.23
)
The following potentially dilutive securities have been excluded from the computations of diluted weighted average shares outstanding because they would be anti-dilutive:
Three Months Ended March 31,
2026
2025
Options to purchase common stock
3,687,269
4,538,059
Warrants to purchase common stock, in connection with April 2023 financing
68,809
68,809
Warrants to purchase common stock, in connection with November 2023 financing
5,805,083
5,805,083
Warrants to purchase common stock, in connection with June 2025 financing
105,726
—
November 2025 convertible notes and PIK interest, if converted
16,801,212
—
Warrants to purchase common stock, in connection with November 2025 financing
65,514,252
—
Warrants to purchase common stock
141,639
196,816
Total potential shares
92,123,990
10,608,767
(13)
Income Taxes
The effective tax rate of
0
% for the three months ended March 31, 2026 and 2025 was lower than the statutory rate due to the Company remaining in a full valuation allowance position.
25
Table of Contents
(14)
Segment Reporting
In accordance with FASB ASC Topic 280,
Segment Reporting
, the Company has determined that it operates as a
single
business segment, which is the development and commercialization of therapeutic and diagnostic products that service women’s reproductive health needs (fertility and permanent birth control).
The determination of a
single
business segment is consistent with the financial information regularly provided to the Company’s chief operating decision maker (“CODM”). As a
single
reportable segment entity, the Company’s segment performance measure is net income (loss) attributable to shareholders. The measurement of segment assets is reported on the balance sheet as total assets. The Company’s CODM is its Chief Executive Officer and Chief Financial Officer, who together review and evaluate net income for purposes of assessing performance, making operating decisions, allocating resources, and planning and forecasting for future periods.
Significant segment expenses, as provided to the CODM are as follows:
Three Months Ended
March 31,
2026
2025
Sales
$
424,889
341,264
Cost of sales (excluding depreciation expense)
158,606
117,266
Research and development expense
438,800
959,162
Other research and development expense 1
870,601
2,009,310
Total research and development expense
1,309,401
2,968,472
Sales and marketing expense
1,315,755
908,567
General and administrative expense
1,782,390
1,722,713
Depreciation and amortization expense
82,270
84,853
Total operating expenses
4,489,816
5,684,605
Total other income (expense), net
5,069,633
(
440,420
)
Income (loss) before income taxes
846,100
(
5,901,027
)
Income tax benefit
—
(
4,188
)
Net income (loss)
$
846,100
(
5,896,839
)
1
Other research and development expense include clinical affairs, regulatory, manufacturing and quality assurance expenses.
(15)
Other Income (expense), net
The company incurred the following Other Income (expense), net for the three months ended March 31, 2026 and 2025:
Three Months Ended
March 31,
2026
2025
Interest income
$
49,827
19,029
Amortization of debt issuance costs and discount for 2025 and 2023 notes
(
176,607
)
(
356,699
)
Interest Expense
—
(
102,750
)
Change in fair value of Conversion Option liability
1,513,413
—
Change in fair value of Warrants liabilities
3,683,000
—
Total other income (expense), net
$
5,069,633
(
440,420
)
26
Table of Contents
(16)
Subsequent Events
On April 29, 2026, at a Special Meeting of Stockholders, shareholders approved a reverse stock split at a ratio in the range of
1-for-2
to
1-for-25
, at the discretion of the board of directors at any time prior to May 1, 2027.
Additionally, at the same meeting, shareholders approved the issuance of shares of common stock issuable upon conversion of the 2025 Notes and exercise of Series A-1, B-1, C-1, and D-1 Warrants, including any issuances to directors and officers of the Company who are holders of these instruments, in excess of
19.99
% of the issued and outstanding shares of common stock of the Company (to the extent that anti-dilution or price adjustment provisions in the instruments result in an effective conversion or exercise price below the Nasdaq Minimum Price).
27
Table of Contents
Item 2.
Management’s Discussion and Analysis of Financial Condition and Results of Operations
The following discussion and analysis of our financial condition and results of operations should be read in conjunction with our financial statements and related notes included elsewhere in this Quarterly Report on Form 10-Q and our Annual Report on Form 10-K filed with the U.S. Securities and Exchange Commission, or the SEC, on March 31, 2026. This Quarterly Report on Form 10-Q contains forward-looking statements within the meaning of Section 27A of the Securities Act of 1933, as amended, and Section 21E of the Securities Exchange Act of 1934, as amended, which are subject to the “safe harbor” created by those sections. Forward-looking statements are based on our management’s beliefs and assumptions and on information currently available to our management. In some cases, you can identify forward-looking statements by terms such as “may,” “will,” “should,” “could,” “goal,” “would,” “expect,” “plan,” “anticipate,” “believe,” “estimate,” “project,” “predict,” “potential” and similar expressions intended to identify forward-looking statements and reflect our beliefs and opinions on the relevant subject. Our actual results could differ materially from those discussed in the forward-looking statements. Factors that could cause or contribute to these differences include those discussed below and elsewhere in this Quarterly Report on Form 10-Q. The forward-looking statements included in this Quarterly Report on Form 10-Q are made only as of the date hereof. These statements are based upon information available to us as of the filing date of this Quarterly Report on Form 10-Q, and while we believe such information forms a reasonable basis for such statements, such information may be limited or incomplete, and our statements should not be read to indicate that we have conducted an exhaustive inquiry into, or review of, all potentially available relevant information. These statements are inherently uncertain, and investors are cautioned not to unduly rely upon these statements.
Overview
We are a leading biomedical innovator, addressing significant unmet needs in women’s health worldwide, with a broad patent-protected portfolio of disruptive, accessible, in-office therapeutic and diagnostic products. The Company is a U.S. manufacturer that has received global regulatory approvals for our product portfolio, which is currently being commercialized in the U.S. and key international markets. FemaSeed® Intratubal Insemination, a groundbreaking first-step infertility treatment delivering sperm directly to the site of conception, is U.S. FDA-cleared and approved in Europe, United Kingdom (“UK”), Canada, Israel, Australia and New Zealand. A peer-reviewed publication of positive data from its pivotal clinical trial of FemaSeed demonstrated effectiveness and safety with high satisfaction from both patients and practitioners. FemSperm
®
, which includes setup, preparation and analysis kits designed to expand our infertility portfolio and, for the first time, enable gynecologists to perform in-office sperm preparation and analysis for use with FemaSeed. FemVue
®
, a companion diagnostic for fallopian tube assessment via ultrasound, is U.S. FDA-cleared and approved in Europe, UK, Canada, Japan, Israel, Australia and New Zealand. FemVue Controlled is a US FDA-cleared diagnostic device and is the next-generation design integrating features of FemVue and FemChec
®
technologies into a single platform, enabling multiple clinical uses within one solution, including confirmation of tubal patency prior to use with FemaSeed. FemCerv
®
, an endocervical tissue sampler for cervical cancer diagnosis, is U.S. FDA-cleared and approved in Europe, UK, Canada, Israel and New Zealand.
28
Table of Contents
FemBloc
®
permanent birth control is a revolutionary first-in-class non-surgical solution which involves minimally-invasive placement of a patented delivery system for precise delivery of our proprietary synthetic tissue adhesive (blended polymer) into both fallopian tubes simultaneously. Over time, the blended polymer fully degrades and produces nonfunctional scar tissue to permanently block the fallopian tubes in a safe and natural approach. This is in stark contrast to centuries-old surgical sterilization with reported risks that include infection, minor or major bleeding, injury to nearby organs, anesthesia-related events, and even death. Along with the various surgical risks, some patients may not qualify as good surgical candidates due to obesity or medical comorbidities. The FemBloc non-surgical approach has the potential to offer a safe and effective, more accessible in-office alternative with fewer risks, contraindications, and substantially lower cost than the surgical alternative. A peer-reviewed publication of positive data from its initial clinical trials of FemBloc has demonstrated compelling effectiveness and five-year safety with high satisfaction from both patients and practitioners. In March 2025, we announced Conformité Européenne (“CE”) mark certification under European Union (“EU”) Medical Device Regulation (“MDR”) as the first regulatory approval in the world for the FemBloc delivery system for non-surgical female permanent birth control and in June 2025, we announced CE mark certification under EU MDR for the class III blended polymer component, achieving approval for the entire FemBloc system in the EU. In August and September 2025, we announced UK and New Zealand regulatory approvals, respectively, for FemBloc. In March and September 2025, we announced strategic distribution partnerships for FemBloc in Spain and France/Benelux region, respectively. We received FDA approval in November 2025 of our investigational device exemption (“IDE”) supplement to move forward to the final phase of the pivotal clinical trial (clinicaltrials.gov: NCT05977751) for U.S. approval. In March 2026, we announced the initiation of enrollment in this final phase. FemChec, a companion diagnostic product for FemBloc’s ultrasound-based confirmation test, is U.S. FDA-cleared and approved in Europe, UK, Canada, Israel, Australia and New Zealand. FemCath
®
for selective fallopian tube evaluation is U.S. FDA-cleared and approved in Europe, Canada and Israel for selective fallopian tube evaluation. We are a woman-founded and led company with an expansive, internally created intellectual property portfolio with approximately 228 issued patents globally, in-house chemistry, manufacturing, and controls (CMC) and device manufacturing capabilities and proven ability to develop products with commercialization efforts underway. Our suite of products and U.S. product candidate address what we believe are multi-billion dollar global market segments in which there has been little advancement for many years, helping women avoid pharmaceutical solutions, implants and surgery that can be expensive and expose women to harm.
Corporate Update
On January 13, 2026, we announced a partnership with Refuah Health Center, advancing adoption of FemaSeed as a first-line infertility treatment in community-based care.
On February 3, 2026, we announced a strategic distribution partnership with OR Consulting to support commercial launch of FemBloc, FemaSeed and other products within the portfolio in Switzerland.
On February 23, 2026, we announced receiving AMA CPT Editorial Panel approval of a new Category III CPT code for FemaSeed intratubal insemination (ITI), supporting future reimbursement pathway.
On February 26, 2026, we announced FemBloc permanent birth control system achieved certification under the Medical Device Single Audit Program (MDSAP), supporting global regulatory readiness.
On March 10, 2026, we announced initiation of patient enrollment in the FINALE pivotal clinical trial evaluating FemBloc, advancing toward U.S. approval.
On March 18, 2026, we appointed Kenneth D. Eichenbaum, M.D., M.S.E., to the Board of Directors.
On April 1, 2026, we announced appointment of John Canning as Chief Operating Officer, who will drive operational execution and support commercial growth.
On April 16, 2026, we announced a strategic partnership with AMI Technologies to introduce and commercialize its fertility portfolio in Israel.
On April 22,2026, we announced the commercial launch of FemaSeed Complete, a comprehensive fertility solution that enables OB/GYNs to perform first-line insemination entirely within their own practices.
On May 5, 2026, we announced enabling OB/GYNs to deliver first-line fertility treatment with initial commercial use of FemaSeed Complete.
29
Table of Contents
Results of Operations
Comparison of the Three Months Ended March 31, 2026 and 2025
The following table shows our results of operations for the three months ended March 31, 2026 and 2025:
Three Months Ended March 31,
2026
2025
Change
% Change
Sales
$
424,889
341,264
83,625
24.5
%
Cost of sales (excluding depreciation expense)
158,606
117,266
41,340
35.3
%
Operating expenses:
Research and development
1,309,401
2,968,472
(1,659,071
)
(55.9
)%
Sales and marketing
1,315,755
908,567
407,188
44.8
%
General and administrative
1,782,390
1,722,713
59,677
3.5
%
Depreciation and amortization
82,270
84,853
(2,583
)
(3.0
)%
Total operating expenses
4,489,816
5,684,605
(1,194,789
)
(21.0
)%
Loss from operations
(4,223,533
)
(5,460,607
)
1,237,074
(22.7
)%
Other income
(expense)
:
Interest income
49,827
19,029
30,798
161.8
%
Change in fair value of conversion option liability
1,513,413
—
1,513,413
100
%
Change in fair value of warrants liabilities
3,683,000
—
3,683,000
100
%
Interest expense
(176,607
)
(459,449
)
282,842
(61.6
)%
Total other income (expense), net
5,069,633
(440,420
)
5,510,053
1,251.1
%
Loss before income taxes
846,100
(5,901,027
)
6,747,127
114.3
%
Income tax benefit
—
(4,188
)
4,188
(100.0
)%
Net income (loss)
$
846,100
(5,896,839
)
6,742,939
114.3
%
Sales
Sales increased by $83,625, or 24.5%, to $424,889 for the three months ended March 31, 2026 from $341,264 for the three months ended March 31, 2025, primarily attributable to sales of FemVue.
Cost of sales
Cost of sales increased by $41,340 or 35.3%, to $158,606 for the three months ended March 31, 2026 from $117,266 for the three months ended March 31, 2025, and is primarily attributed to increased sales.
Research and development
The following table summarizes our R&D expenses incurred during the periods presented:
Three Months Ended March 31,
2026
2025
Compensation and related personnel costs
$
890,326
1,305,659
Clinical-related costs
254,712
393,975
Material and development costs
94,609
541,499
Professional and outside consultant costs
56,124
192,196
Regulatory and other costs
13,630
535,143
Total research and development expenses
$
1,309,401
2,968,472
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R&D expenses decreased by $1,659,071 or 55.9%, to $1,309,401 for the three months ended March 31, 2026 from $2,968,472 for the three months ended March 31, 2025. The decrease primarily reflects the transition of development products into inventory to support commercialization, along with lower development, clinical, compensation and professional service costs.
Sales and marketing
Sales and marketing expenses increased by $407,188 or 44.8%, to $1,315,755 for the three months ended March 31, 2026 from $908,567 for the three months ended March 31, 2025. The increase resulted primarily from higher compensation costs, professional fees and travel expenses.
General and administrative
General and administrative expenses increased by $59,677, or 3.5%, to $1,782,390 for the three months ended March 31, 2026 from $1,722,713 for the three months ended March 31, 2025. The increase resulted primarily from increased professional fees, offset by reduced compensation costs.
Depreciation and amortization
Depreciation and amortization expenses decreased by $2,583, or 3.0%, to $82,270 for the three months ended March 31, 2026 from $84,853 for the three months ended March 31, 2025. The decrease resulted from certain fixed assets reaching the end of their useful lives and no longer depreciating.
Other income (expense), net
Other income (expense), net increased by $5,510,053 or 1,251.1%, to $5,069,633 for the three months ended March 31, 2026 from $440,420 for the three months ended March 31, 2025. The increase resulted from the change in fair value on the Conversion Option liability and Warrants liabilities, interest income earned on our cash and cash equivalents and reduced non-cash interest expense related to amortization for our convertible note. Refer to table below for further details.
Three Months Ended
March 31,
2026
2025
Interest income
$
49,827
19,029
Amortization of debt issuance costs and discount for 2025 Notes
(176,607
)
—
Amortization of debt issuance costs and discount for 2023 Notes
—
(356,699
)
Interest expense
—
(102,750
)
Change in fair value of Conversion Option liability
1,513,413
—
Change in fair value of Warrants liabilities
3,683,000
—
Total other income (expense), net
$
5,069,633
(440,420
)
Income tax benefit
Income tax benefit decreased by $4,188 or 100%, to $0 for the three months ended March 31, 2026 from $4,188 for the three months ended March 31, 2025 due to an estimation of lower income tax expense in the first quarter of 2026 compared to 2025.
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Liquidity and Capital Resources
Sources of liquidity
Since our inception through March 31, 2026, our operations have been financed primarily by net proceeds from the sale of our common stock and convertible preferred stock, indebtedness and, to a lesser extent, product revenue. As of March 31, 2026, we had $5,386,041 of cash and cash equivalents and an accumulated deficit of $144,980,044.
In July 2022, we entered into an Equity Distribution Agreement with Piper Sandler & Co. (the “Sales Agent”) and filed a related prospectus establishing an “at-the-market” facility, pursuant to which we may offer and sell shares of our common stock from time to time through the Sales Agent. In December 2025, we filed a new prospectus pursuant to which we may sell up to $9.8 million under the Equity Distribution Agreement. As of March 31, 2026, approximately 624,000 shares of common stock had been sold for aggregate proceeds of approximately $353,000 under the Equity Distribution Agreement pursuant to the prospectus. As of March 31, 2026, the amount we were authorized to sell was subject to baby-shelf limitations. As of March 31, 2026, the available amount pursuant to the prospectus was approximately $9.5 million.
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In June 2025, we sold 3,600,000 shares of common stock in an underwritten public offering at $0.85 per share. Separately and concurrently, we sold 1,686,275 shares of common stock in a private placement at a price of $0.85 per share to certain existing institutional stockholders and a price of $1.02 per share to certain directors and officers. Net proceeds from the transaction were $3,705,061.
On June 30, 2025, we entered into an Any Market Purchase Agreement (“Purchase Agreement” or “AMPA”) with Alumni Capital LP (“Alumni”) whereby we have the right, but not obligation, to sell to Alumni up to an aggregate of $10 million in shares of common stock in a series of purchases until December 31, 2026. We may elect that Alumni purchase up to $1 million in shares of common stock (or up to $5 million if mutually agreed) at either (i) the lowest traded price for 4 previous business days, multiplied by 90%, or (ii) up to the lesser of (a) $1 million in shares of common stock, or (b) 100% of the average daily trading volume of common stock for previous two business days at lowest daily dollar volume-weighted average price, multiplied by 97%. We are limited to issuances to Alumni or 19.99% of the shares of common stock outstanding immediately prior to the execution of the Purchase Agreement.
In August 2025, we sold an aggregate of (i) 10,434,586 shares of common stock in a public offering and to certain Company officers (ii) pre-funded warrants to purchase up to 11,750,000 shares of common stock and (iii) common warrants to purchase up to 22,184,586 shares of common stock. Additionally, common warrants to purchase 443,692 shares of common stock were issued to the underwriter as compensation for services performed. The purchase price per share for the common stock was $0.36, except for shares sold to certain company officers, which was $0.5151 per share. The purchase price per share for the pre-funded warrants was $0.3599. The net proceeds from the August 2025 Financing at closing were approximately $7.1 million. As of March 31, 2026, 5,000,000 pre-funded warrants and 9,219,110 common warrants were exercised for approximately $3.3 million.
In November 2025, we entered into a definitive agreement for the issuance of (i) senior secured convertible notes in an aggregate principal amount of $12,000,000, convertible into shares of 16,378,563 common stock at a conversion price of $0.73 per share, (ii) Series A-1 Warrants to purchase up to an aggregate of 16,378,563 shares of common stock at an exercise price of $0.81 per share, subject to adjustments (iii) Series B-1 Warrants to purchase an aggregate of 16,378,563 shares of common stock at an exercise price of $0.92 per share, subject to adjustments, and (iv) Series C-1 Warrants to purchase an aggregate of 16,378,563 shares of common stock at an exercise price of $1.10 per share, subject to adjustments. The financing resulted in aggregate gross proceeds of $12,000,000, with total potential funding of approximately $58 million, if all warrants are exercised for cash. In March 2026, we modified the November 2025 agreement to remove the non-standard adjustment to the conversion price of the notes and exercise prices of the Series A-1 Warrants, Series B-1 Warrants and Series C-1 Warrants, respectively, upon a Share Combination Event. As consideration for this modification, the Company issued the holders of the 2025 Notes and related Warrants new Series D-1 Warrants which allow the holders to purchase an aggregate number of 16,378,563 shares of the Company’s common stock at an exercise price of $0.58 per share.
Funding requirements
Based on our current operating plan, our current cash and cash equivalents and anticipated revenues from product sales are expected to be sufficient to fund our ongoing operations into the third quarter of 2026. However, it is not sufficient to fund our ongoing operations for twelve months from the date of these financial statements and we will need to obtain additional financing to fund our ongoing operations. Our convertible notes contain restrictions that limit our ability to issue securities without complying with certain participation rights. Our estimate as to how long we expect our existing cash and cash equivalents to be able to continue to fund our operations is based on assumptions that may prove to be wrong, and we could use our available capital resources sooner than we currently expect. Changing circumstances, some of which may be beyond our control, could cause us to consume capital significantly faster than we currently anticipate. As a result of our current limited financial liquidity, we have concluded that substantial doubt exists about our ability to continue as a going concern.
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Our cash and cash equivalents as of March 31, 2026, anticipated revenues from product sales will not be sufficient to sustain our operations, including funding our U.S. product candidate, FemBloc through regulatory approval, and we will need to raise additional capital to complete the U.S. development and EU commercialization of our product candidate and U.S. commercialization of our fertility portfolio, including FemaSeed. However, we can give no assurances that we will be able to secure additional sources of funds to support our commercialization efforts or operations, or if such funds will be available to us, that such additional financing will be sufficient to meet our needs or be on terms acceptable to us. This risk may increase if economic and market conditions deteriorate. If we are unable to obtain additional financing when needed, we may need to terminate, significantly modify, or delay the development of our U.S. product candidate, or we may need to obtain funds through collaborations or otherwise on terms that may require us to relinquish rights to our technologies or our U.S. product candidate that we might otherwise seek to develop or commercialize independently. If we are unable to raise adequate additional capital as and when required in the future, we could be forced to cease development and commercialization activities and terminate our operations, and you could experience a complete loss of your investment.
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We expect to continue to make substantial investments in our ongoing commercialization of our products and the pivotal trial that is designed to provide clinical evidence of the safety and effectiveness of our U.S. product candidate, FemBloc. We also expect to continue to make investments in research and development to develop future products, manufacturing, regulatory affairs and post-market clinical trials. We will additionally need to make investments in our sales and marketing organization for FemaSeed and FemBloc. Because of these and other factors, we expect to continue to incur substantial net losses and negative cash flows from operations for the foreseeable future.
Our future capital requirements will depend on many factors, including:
•
the cost, timing and results of our clinical trial and U.S. regulatory reviews;
•
the cost and timing of establishing sales, marketing, and distribution capabilities;
•
the timing, receipt, and amount of sales from our current and potential products;
•
our ability to continue manufacturing our products and U.S. product candidate and to secure the components, services, and supplies needed in their production;
•
the degree of success we experience in commercializing our products;
•
the emergence of competing or complementary technologies;
•
the cost of preparing, filing, prosecuting, maintaining, defending, and enforcing any patent claims and other intellectual property rights; and
•
the extent to which we acquire or invest in businesses, products, or technologies, although we currently have no commitments or agreements relating to any of these types of transactions.
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Cash Flows
Comparison of the Three Months Ended
March
31, 2026 and 2025
The following table summarizes our cash flows for the three months ended March 31, 2026 and 2025:
Three Months Ended March 31,
2026
2025
Net cash used in operating activities
$
(4,143,508
)
(4,765,214
)
Net cash used in investing activities
(79,138
)
(96,605
)
Net cash provided by financing activities
342,334
5,230,266
Net change in cash and cash equivalents
$
(3,880,312
)
368,447
Operating activities
For the three months ended March 31, 2026, cash used in operating activities was $4,143,508, attributable to net income of $846,100, offset by net non-cash gains of $4,667,748 and a net change in our net operating assets and liabilities of $321,860. Non-cash activity primarily consisted of a change in fair value of the Conversion Option liability and warrants liabilities of $1,513,413 and $3,683,000, respectively, $176,607 of amortization of the discount on convertible notes, $151,608 in share-based compensation, $118,180 in right-of-use asset amortization and $82,270 in depreciation and amortization. The change in our net operating assets and liabilities was primarily due to an increase in inventory of $365,018, decreases in accounts payable of $253,439, accrued expenses of $193,226, lease liabilities of $125,280, offset by a decrease in accounts receivable of $444,336 and decreases in prepaid and other assets of $168,722. We intend to meet future operating cash requirements through increased sales of commercial products and fundraising, as discussed in
Funding requirements
.
Funding requirements
.
For the three months ended March 31, 2025, cash used in operating activities was $4,765,214, attributable to a net loss of $5,896,839, partially offset by non-cash charges of $984,503 and a net change in our net operating assets and liabilities of $147,122. Non-cash charges primarily consisted of $367,237 in share-based compensation, $356,699 in amortization of the discount on convertible notes, $132,207 in right-of-use asset amortization and $84,853 in depreciation and amortization. The change in our net operating assets and liabilities was primarily due to a decrease in accounts receivable of $254,775 and an increase in accounts payable and accrued expenses of $909,917, partially offset by an increase in inventory of $815,865, a decrease in lease liabilities of $133,076 and increase in prepaid and other assets of $53,523. The Company intends to meet future operating cash requirements through increased sales of commercial products and fundraising, as discussed in
Funding requirements
.
Investing activities
For the three months ended March 31, 2026, cash used in investing activities for the purchase of property and equipment was $79,138.
For the three months ended March 31, 2025, cash used in investing activities for the purchase of property and equipment was $96,605.
Financing activities
For the three months ended March 31, 2026, cash provided by financing activities was $342,334, attributable to proceeds from sales under the at-the-market facility, net of issuance costs.
For the three months ended March 31, 2025, cash provided by financing activities was $5,230,266, attributable to proceeds from sales under the at-the-market facility, net of issuance costs.
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Critical Accounting Estimates
Management’s discussion and analysis of our financial condition and results of operations is based on our financial statements, which have been prepared in accordance with U.S. generally accepted accounting principles, or GAAP. The preparation of these financial statements requires us to make estimates and assumptions for the reported amounts of assets, liabilities, revenue, expenses and related disclosures. Our estimates are based on our historical experience and on various other factors that we believe are reasonable under the circumstances, the results of which form the basis for making judgments about the carrying value of assets and liabilities that are not readily apparent from other sources. Actual results may differ from these estimates under different assumptions or conditions and any such differences may be material.
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While our significant accounting policies are more fully described in Note 2 to our financial statements appearing in the Annual Report on Form 10-K for the year ended December 31, 2025 as filed on March 31, 2026, we believe the following discussion addresses our most critical accounting policies, which are those that are most important to our financial condition and results of operations and require our most difficult, subjective and complex judgments.
Revenue recognition
Our policy is to recognize revenue when a customer obtains control of the promised goods under Accounting Standards Update (ASU) 2020-05,
Revenue from Contracts with Customers
(Topic 606), which we adopted effective January 1, 2018. The amount of revenue recognized reflects the consideration to which we expect to be entitled to receive in exchange for these goods, and we have elected to exclude amounts collected from customers for all sales (and other similar) taxes from the transaction price. We do not have multiple performance obligations in our customer orders, so revenue is recognized upon shipment of our goods based upon contractually stated pricing at standard payment terms typically ranging from 30 to 60 days. All revenue is recognized at a point in time.
The majority of products sold directly to U.S. customers are shipped via common carrier, and the customer pays for shipping and handling and assumes control at Free on Board (FOB) shipping point. Products shipped to our international distributors are in accordance with their respective agreements; however, the shipping terms are generally EX-Works, reflecting that control is assumed by the distributor at the shipping point. Returns are only accepted with prior authorization from us. Items to be returned must be in original unopened cartons and are subject to a 30% restocking fee. As of March 31, 2026, we have not had a history of significant returns.
Convertible Notes, Conversion Option liability and Warrants liabilities
The Company accounts for debt and equity instruments issued in financing transactions, including the senior secured convertible notes (“2025 Notes”) and related warrants issued in its November 2025 financing transaction, using significant judgments and estimates. The financial instruments issued contain complex embedded features, including conversion options, exercise price adjustment provisions, redemption features, and other settlement terms that require evaluation under applicable accounting guidance to determine whether such features should be classified as equity or as derivative liabilities.
Management concluded that certain embedded conversion features within the 2025 Notes and the related warrants were not indexed to the Company’s common stock under ASU 815-40 and did not qualify for equity classification, primarily due to shareholder approval requirements that limited settlement in shares and, prior to the March 2026 modification, certain market-based adjustment provisions. Accordingly, the conversion option embedded in the 2025 Notes and the warrants were recognized as derivative liabilities and initially recorded at fair value in accordance with ASC 820, with subsequent changes in fair value recognized in earnings each reporting period.
In March 2026, the Company modified the 2025 Notes and related warrants to remove certain market-based adjustment provisions and issued additional Series D-1 warrants in connection with the modification. The Company evaluated the modification under applicable accounting guidance and recorded the new Series D-1 warrants as derivative liabilities at fair value upon issuance.
The valuation of the derivative liabilities requires the use of significant estimates and assumptions, including the Company’s stock price, expected volatility, expected term, risk-free interest rates, probability and timing of potential future events, and assumptions related to conversion and exercise probability. Changes in these assumptions could materially impact the estimated fair value of the derivative liabilities and the related gains or losses recognized in the Company’s statements of comprehensive income (loss).
In addition, the Company records the 2025 Notes at amortized cost and accretes the associated debt discount and issuance costs to interest expense using the effective interest method over the expected term of the instruments. The effective interest rate of the 2025 Notes was impacted by the initial allocation of proceeds between the debt host and derivative liabilities which required significant management judgment.
Item 3.
Quantitative and Qualitative Disclosures About Market Risk
Not applicable.
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Item 4.
Controls and Procedures
Evaluation of Disclosure Controls and Procedures
We maintain disclosure controls and procedures that are designed to ensure that information required to be disclosed in the reports that we file or submit under the Exchange Act is (1) recorded, processed, summarized and reported within the time periods specified in the SEC’s rules and forms, and (2) accumulated and communicated to our management, including to our principal executive officer and principal financial officer, to allow timely decisions regarding required disclosure. Our management, with the participation of our Chief Executive Officer (principal executive officer) and Chief Financial Officer (principal financial and accounting officer), has evaluated the effectiveness of our disclosure controls and procedures (as defined in Rules 13a-15(e) and 15d-15(e) under the Securities Exchange Act of 1934, as amended) as of the end of the period covered by this Quarterly Report on Form 10-Q. Based on such evaluation, our management has concluded that our disclosure controls and procedures were effective at a reasonable assurance level as of March 31, 2026.
Changes in Internal Control over Financial Reporting
There were no changes in our internal control over financial reporting identified in connection with the evaluation required by Rule 13a-15(d) and 15d-15(d) of the Exchange Act that occurred during the quarter ended March 31, 2026 that have materially affected, or are reasonably likely to materially affect, our internal control over financial reporting.
Inherent Limitations on Effectiveness of Controls
Our management, including our Chief Executive Officer (principal executive officer) and Chief Financial Officer (principal financial and accounting officer), does not expect that our disclosure controls and procedures or internal control over financial reporting will prevent all errors and all fraud. A control system, no matter how well designed and implemented, can provide only reasonable, not absolute, assurance that the control system’s objectives will be met. Further, the design of a control system must reflect the fact that there are resource constraints, and the benefits of controls must be considered relative to their costs. Because of the inherent limitations in all control systems, no evaluation of controls can provide absolute assurance that all control issues within a company are detected. The inherent limitations include the realities that judgments in decision-making can be faulty and that breakdowns can occur because of simple errors or mistakes. Controls can also be circumvented by the individual acts of some persons, by collusion of two or more people, or by management override of the controls. Also, projections of any evaluation of effectiveness to future periods are subject to the risk that controls may become inadequate because of changes in conditions or that the degree of compliance with the policies or procedures may deteriorate. Because of the inherent limitations in a cost-effective control system, misstatements due to error or fraud may occur and may not be detected.
PART II OTHER INFORMATION
Item 1.
Legal Proceedings
From time to time we may be involved in legal proceedings arising in connection with our business. As of March 31, 2026, we have not had a history of significant legal proceedings and there are no currently pending actions against us. We believe that any amount, or range, of reasonably possible losses in connection with any potential actions against us in excess of established reserves, in the aggregate, will not be material to our financial condition or cash flows. However, losses may be material to our operating results for any particular future period, depending on the level of income for such period and the significance of any actions against us.
Item 1A.
Risk Factors
As of the date of this report, there are no material changes to our risk factors as previously disclosed in Part I, Item 1A of our Annual Report on Form 10-K for the year ended December 31, 2025 except as noted below.
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We have received deficiency letters from Nasdaq relating to our non-compliance with Nasdaq’s continued listing requirements and our common stock could become subject to delisting from Nasdaq if we fail to regain compliance.
On May 19, 2025, we received a written notice (the “Notice”) from The Nasdaq Stock Market LLC (“Nasdaq”) that for the last 30 consecutive business days, the Market Value of Listed Securities (“MVLS”) for our common stock was below the minimum $35.0 million requirement for continued listing on The Nasdaq Capital Market pursuant to Nasdaq Listing Rule 5550(b)(2) (the “Minimum MVLS Requirement”). Additionally, we did not meet either of the alternative Nasdaq continued listing standards under Nasdaq Listing Rule 5550(b)(2): (i) stockholders’ equity of at least $2.5 million or (ii) net income of $500,000 in the most recently completed fiscal year, or in two of the three most recently completed fiscal years.
Following the completion of our August 2025 financing and subsequent warrant exercises, we determined that our stockholders' equity as of October 15, 2025 would have been approximately $5.2 million on a pro forma basis, meeting the minimum $2.5 million stockholders' equity requirement for continued listing under Nasdaq Listing Rule 5550(b)(1). As reported on our Form 8-K filed October 21, 2025, and as further evidenced in our Annual Report on Form 10-K for the fiscal year ended December 31, 2025, Nasdaq determined that we are in compliance with Nasdaq Listing Rule 5550(b)(1). However, if we fail to evidence continued compliance in any subsequent periodic report, we may again become subject to a deficiency determination and potential delisting proceedings.
On July 16, 2025, we received a notice from Nasdaq that the Company was not in compliance with Nasdaq Listing Rule 5550(a)(2), as the minimum bid price of the Company’s common stock had been below $1.00 per share for 30 consecutive business days (the “Minimum Bid Price Requirement”).
In accordance with Nasdaq Listing Rule 5810(c)(3)(A), we have a period of 180 calendar days, or until January 12, 2026, to regain compliance with the Minimum Bid Price Requirement. To regain compliance, the minimum bid price of the Company’s common stock must meet or exceed $1.00 per share for a minimum of ten consecutive business days during this 180-calendar day grace period. In the event the Company does not regain compliance with the Minimum Bid Price Requirement by January 12, 2026, the Company may be eligible for an additional 180-calendar day compliance period if it meets all other initial listing standards for The Nasdaq Capital Market, with the exception of the Minimum Bid Price Requirement, and provides written notice of its intention to cure the bid deficiency during the second compliance period, by effecting a reverse stock split, if necessary. If the Company does not regain compliance with the Minimum Bid Price Requirement by the end of the compliance period (or the second compliance period, if applicable), the Company’s common stock will become subject to delisting. In the event that the Company receives notice that its common stock is being delisted, the Nasdaq listing rules permit the Company to appeal a delisting determination by the Staff to a hearings panel.
On January 12, 2026, we submitted a request to Nasdaq for a 180-day extension, advising Nasdaq that we had demonstrated more than $5 million in stockholders' equity as of December 31, 2025 and providing notice of our intention to cure the deficiency during the extended compliance period by effecting a reverse stock split, if necessary. On January 13, 2026, Nasdaq granted us a second 180-day extension through July 13, 2026 to regain compliance with the Minimum Bid Price Requirement. This is the final compliance period available to us under Nasdaq's rules. If we do not regain compliance by July 13, 2026, our common stock will become subject to delisting. In the event we receive notice that our common stock is being delisted, Nasdaq's rules permit us to appeal that determination to a hearings panel, although no assurance can be given that any such appeal would be successful. On April 29, 2026, our stockholders approved a reverse stock split of our common stock at a ratio in the range of 1-for-2 to 1-for-25, with such ratio as determined at the discretion of the board of directors at any time prior to May 1, 2027. We intend to continue actively monitoring the closing bid price of our common stock and will consider all available options to regain compliance, including effecting a reverse stock split. However, there can be no assurance that we will be able to regain compliance with the Minimum Bid Price Requirement by July 13, 2026, maintain compliance with the stockholders' equity requirement, or remain in compliance with other Nasdaq listing rules. If our common stock is delisted, it could have a material adverse effect on the price and liquidity of our common stock and our ability to raise additional capital.
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We intend to monitor the closing bid price of our common stock and may, if appropriate, consider available options to regain compliance with the Minimum Bid Price Requirement, including effecting the reverse stock split since approved by our stockholders at the Special Meeting. However, there can be no assurance that we will be able to regain compliance with the Minimum Bid Price Requirement or will otherwise be in compliance with other Nasdaq Listing Rules.
If we effect a reverse stock split to regain compliance with the Nasdaq Minimum Bid Price Requirement, it may not result in a sustained increase in the market price of our common stock, may trigger significant dilution to our stockholders, and could have other material adverse consequences.
If we effect a reverse stock split, the market price of our common stock following such split may not be proportionate to the ratio of the split, and any increase in our stock price resulting from the reverse stock split may not be sustained. The market price of our common stock is determined by a variety of factors, many of which are unrelated to the number of shares outstanding. A reverse stock split has frequently been followed by a decline in the stock price of the affected company, and there can be no assurance that our stock price will not decline below $1.00 per share following any reverse stock split we may effect, which would subject us to renewed Nasdaq non-compliance and potential delisting proceedings.
Furthermore, even if we regain compliance with the Nasdaq Minimum Bid Price Requirement by effecting a reverse stock split, we may fail to remain in compliance with other Nasdaq continued listing standards, including the minimum stockholders' equity requirement of $2.5 million under Nasdaq Listing Rule 5550(b)(1). If our common stock is delisted from Nasdaq, it could have a material adverse effect on the price and liquidity of our common stock, our ability to raise additional capital, and the value of your investment.
We need substantial additional funding and may be unable to raise capital when needed, which could force us to delay or reduce our commercialization efforts or product development programs.
Based on our current operating plan, our current cash, cash equivalents and revenue are expected to be sufficient to fund our ongoing operations into the third quarter of 2026. However, we have based these estimates on assumptions that may prove to be incorrect, and we could spend our available financial resources much faster than we currently expect. Any future funding requirements will depend on many factors, including:
•
The initiation, scope, rate of enrollment, progress, success, and cost of our current or future clinical trials;
•
The cost of our research and development activities;
•
Patient, healthcare practitioner and market acceptance of our intratubal insemination product and permanent birth control system, both women-specific medical product solutions;
•
The cost of filing and prosecuting patent applications and defending and enforcing our patent or other intellectual property rights;
•
The cost of defending, in litigation or otherwise, any claims that we infringe third-party patents or other intellectual property rights;
•
The cost and timing of additional regulatory clearances or approvals;
•
The cost and timing of establishing additional sales and marketing capabilities;
•
Costs associated with any product recall that may occur;
•
The effect of competing technological and market developments;
•
The extent to which we acquire or invest in products, technologies and businesses, although we currently have no commitments or agreements relating to any of these types of transactions; and
•
The costs of operating as a public company.
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We still need significant additional financing to fund our product development and operations. Any additional equity or debt financing that we raise may contain terms that are not favorable to us or our stockholders. If we raise additional funds by selling additional shares of our common stock or other securities convertible into or exercisable or exchangeable for shares of our common stock, the issuance of such securities will result in dilution to our stockholders. Certain equity capital raisings may trigger price adjustments to the warrants issued in November 2025 and March 2026. Furthermore, investors purchasing any securities we may issue in the future may have rights superior to the rights of our common stockholders.
In addition, any future debt financing into which we enter may impose upon us covenants that restrict our operations, including limitations on our ability to incur liens or additional debt, pay dividends, repurchase our common stock, make certain investments and engage in certain merger, consolidation or asset sale transactions. Our convertible notes contain restrictions that limit our ability to issue securities without complying with certain participation rights. If we raise additional funds through collaboration and licensing arrangements with third-parties, it may be necessary to relinquish some rights to our technologies or our products, or grant licenses on terms that are not favorable to us.
Furthermore, we cannot be certain that additional funding will be available on acceptable terms, if at all. If we do not have, or are not able to obtain, sufficient funds, we may have to delay development or commercialization of our products or license to third-parties the rights to commercialize products or technologies that we would otherwise seek to commercialize. We also may have to reduce commercialization efforts, customer support or other resources devoted to our products or cease operations. Any of these factors could harm our business, financial condition, and results of operations.
Item 2.
Unregistered Sales of Equity Securities, Use of Proceeds, and Issuer Purchases of Equity Securities
None.
Item 3.
Defaults Upon Senior Securities
None.
Item 4.
Mine Safety Disclosures
Not applicable.
Item 5.
Other Information
During the period covered by this Quarterly Report,
none
of our directors or executive officers have adopted or terminated a Rule 10b5-1 trading arrangement or a non-Rule 10b5-1 trading arrangement (each as defined in Item 408 of Regulation S-K under the Securities Exchange Act of 1934, as amended).
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Item 6.
Exhibits
Incorporated by
Reference
Exhibit
Number
Description of Document
Schedule/Form
File
Number
Exhibit
Filing
Date
3.1
Eleventh Amended and Restated Certificate of Incorporation of Femasys Inc.
Form 8-K
001-40492
3.1
June 22, 2021
3.2
Amended and Restated Bylaws of Femasys Inc.
Form 8-K
001-40492
3.2
June 22, 2021
3.3
First Amendment to the Amended and Restated Bylaws of Femasys Inc.
Form 8-K
001-40492
3.1
March 30, 2023
4
Form of Series D-1 Warrant
Form 8-K
001-40492
4.1
March 20, 2026
10.1
Omnibus Amendment and Consent Agreement
Form 8-K
001-40492
10.1
March 20, 2026
10.2
Employment Agreement, dated as of March 30, 2026, between Femasys Inc. and John Canning
Form 8-K
001-40492
10.1
April 1, 2026
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31.1*
Certification of Principal Executive Officer Pursuant to Securities Exchange Act Rules 13a-14(a), as adopted Pursuant to Section 302 of the Sarbanes-Oxley Act of 2002
31.2*
Certification of Principal Financial Officer Pursuant to Securities Exchange Act Rules 13a-14(a), as adopted Pursuant to Section 302 of the Sarbanes-Oxley Act of 2002
32.1*
Certification of Principal Executive Officer Pursuant to 18 U.S.C. Section 1350, as adopted Pursuant to Section 906 of the Sarbanes-Oxley Act of 2002
32.2*
Certification of Principal Financial Officer Pursuant to 18 U.S.C. Section 1350, as adopted Pursuant to Section 906 of the Sarbanes-Oxley Act of 2002
101.INS*
Inline XBRL Instance Document (the instance document does not appear in the Interactive Data File because its XBRL tags are embedded within the Inline XBRL document)
101.SCH*
Inline XBRL Taxonomy Extension Schema Document
101.CAL
Inline XBRL Taxonomy Extension Calculation Linkbase Document
101.DEF*
Inline XBRL Taxonomy Definition Linkbase Document
101.LAB*
Inline XBRL Taxonomy Extension Label Linkbase Document
101.PRE*
Inline XBRL Taxonomy Extension Presentation Linkbase Document
104*
Cover Page Interactive Data File (formatted as inline XBRL and contained in Exhibit 101)
*Filed herewith
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SIGNATURES
Pursuant to the requirements of the Securities Exchange Act of 1934, the registrant has duly caused this report to be signed on its behalf by the undersigned, thereunto duly authorized, in the City of Suwanee, State of Georgia, on this 8
th
day of May 2026.
FEMASYS INC
Dated: May 8, 2026
By: /s/ Kathy Lee-Sepsick
Kathy Lee-Sepsick
Chief Executive Officer and President
Dated: May 8, 2026
By: /s/ Dov Elefant
Dov Elefant
Chief Financial Officer
2024-11-30
2035-11-30
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2024-11-30
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