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Watchlist
Account
Apyx Medical
APYX
#8891
Rank
$0.15 B
Marketcap
๐บ๐ธ
United States
Country
$3.68
Share price
1.38%
Change (1 day)
268.00%
Change (1 year)
Medical devices
Categories
Market cap
Revenue
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P/E ratio
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Price history
P/E ratio
P/S ratio
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Total assets
Total liabilities
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Cash on Hand
Net Assets
Annual Reports (10-K)
Apyx Medical
Quarterly Reports (10-Q)
Financial Year FY2023 Q2
Apyx Medical - 10-Q quarterly report FY2023 Q2
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UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
Washington, D.C. 20549
FORM
10-Q
☒
QUARTERLY REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934
For the quarterly period ended
June 30, 2023
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:
0-12183
APYX MEDICAL CORPORATION
(Exact name of registrant as specified in its charter)
Delaware
11-2644611
(State or other jurisdiction of
incorporation or organization)
(I.R.S. Employer
Identification No.)
5115 Ulmerton Road,
Clearwater
,
FL
33760
(Address of principal executive offices, zip code)
(
727
)
384-2323
(Registrant’s telephone number)
Securities Registered Pursuant to Section 12 (b) of the Act:
Title of each class
Trading symbol(s)
Name of each exchange on which registered
Common Stock
APYX
Nasdaq Stock Market, LLC
Indicate by check mark whether the registrant (1) 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 (§232.405 of this chapter) 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, a smaller reporting company, or an emerging growth company. See the definitions of “large accelerated filer”, “accelerated filer”, “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
☒
A
s
of August 9, 2023,
34,643,855
shares of the registrant’s $0.001 par value common stock were outstanding.
Table of Contents
APYX MEDICAL CORPORATION
INDEX TO QUARTERLY REPORT ON FORM 10-Q
For the quarterly period ended June 30, 2023
Page
Part I.
Financial Information
2
Item 1.
Condensed Consolidated
Financial Statements
(Unaudited)
2
Condensed
Consolidated Balance Sheets at
June 30, 2023 and December 31, 2022
2
Condensed
Consolidated Statements of Operations for the three
and six months ended June 30, 2023 and 2022
3
Condensed
Consolidated Statements of Changes in Equity for the
three and six months ended June 30, 2023 and 2022
4
Condensed Consolidated Statements of Cash Flows for the six months ended June 30, 2023 and 2022
5
Notes to Condensed Consolidated Financial Statements
6
Item 2.
Management’s Discussion and Analysis of Financial Condition and Results of Operations
23
Item 3.
Quantitative and Qualitative Disclosures about Market Risk
34
Item 4.
Controls and Procedures
35
Part II.
Other Information
36
Item 1.
Legal Proceedings
36
Item 1A.
Risk Factors
37
Item 2.
Unregistered Sales of Equity Securities and Use of Proceeds
38
Item 3.
Defaults Upon Senior Securities
38
Item 4.
Mine Safety Disclosures
38
Item 5.
Other Information
38
Item 6.
Exhibits
39
Signatures
40
1
Table of Contents
PART I. Financial Information
ITEM 1. Condensed Consolidated Financial Statements
APYX MEDICAL CORPORATION
CONDENSED CONSOLIDATED BALANCE SHEETS
(In thousands, except share and per share data)
June 30, 2023
(Unaudited)
December 31, 2022
ASSETS
Current assets:
Cash and cash equivalents
$
18,479
$
10,192
Trade accounts receivable, net of allowance of $
555
and $
668
12,072
10,602
Income tax receivables
7,752
7,545
Other receivables
315
99
Inventories, net of provision for obsolescence of $
579
and $
457
11,167
11,797
Prepaid expenses and other current assets
3,100
2,737
Total current assets
52,885
42,972
Property and equipment, net
2,118
6,761
Operating lease right-of-use assets
5,421
710
Finance lease right-of-use assets
97
115
Other assets
1,908
1,217
Total assets
$
62,429
$
51,775
LIABILITIES AND EQUITY
Current liabilities:
Accounts payable
$
2,658
$
2,669
Accrued expenses and other current liabilities
7,114
8,928
Current portion of operating lease liabilities
337
216
Current portion of finance lease liabilities
28
37
Term loan, net
8,892
—
Total current liabilities
19,029
11,850
Long-term operating lease liabilities
5,093
470
Long-term finance lease liabilities
63
73
Long-term contract liabilities
1,326
1,408
Other liabilities
185
181
Total liabilities
25,696
13,982
EQUITY
Preferred stock, $
0.001
par value;
10,000,000
shares authorized;
0
issued and outstanding as of June 30, 2023 and December 31, 2022
—
—
Common stock, $
0.001
par value;
75,000,000
shares authorized;
34,628,517
issued and outstanding as of June 30, 2023, and
34,597,822
issued and outstanding as of December 31, 2022
35
35
Additional paid-in capital
76,773
73,282
Accumulated deficit
(
40,212
)
(
35,735
)
Total stockholders’ equity
36,596
37,582
Non-controlling interest
137
211
Total equity
36,733
37,793
Total liabilities and equity
$
62,429
$
51,775
The accompanying notes are an integral part of the condensed consolidated financial statements.
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Table of Contents
APYX MEDICAL CORPORATION
CONDENSED CONSOLIDATED STATEMENTS OF OPERATIONS
(Unaudited)
(In thousands, except per share data)
Three Months Ended
June 30,
Six Months Ended
June 30,
2023
2022
2023
2022
Sales
$
13,569
$
10,292
$
25,711
$
22,785
Cost of sales
4,290
3,378
8,859
7,652
Gross profit
9,279
6,914
16,852
15,133
Other costs and expenses:
Research and development
1,199
1,070
2,320
2,228
Professional services
1,594
2,389
3,334
4,675
Salaries and related costs
5,035
4,892
10,103
10,073
Selling, general and administrative
5,378
4,539
10,633
10,004
Total other costs and expenses
13,206
12,890
26,390
26,980
Gain on sale-leaseback
2,692
—
2,692
—
Loss from operations
(
1,235
)
(
5,976
)
(
6,846
)
(
11,847
)
Interest income
179
18
230
20
Interest expense
(
543
)
(
3
)
(
777
)
(
11
)
Other income, net
646
607
641
586
Total other income, net
282
622
94
595
Loss before income taxes
(
953
)
(
5,354
)
(
6,752
)
(
11,252
)
Income tax expense (benefit)
66
96
(
2,201
)
166
Net loss
(
1,019
)
(
5,450
)
(
4,551
)
(
11,418
)
Net loss attributable to non-controlling interest
(
25
)
(
24
)
(
74
)
(
47
)
Net loss attributable to stockholders
$
(
994
)
$
(
5,426
)
$
(
4,477
)
$
(
11,371
)
Loss per share:
Basic and diluted
$
(
0.03
)
$
(
0.16
)
$
(
0.13
)
$
(
0.33
)
The accompanying notes are an integral part of the condensed consolidated financial statements.
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APYX MEDICAL CORPORATION
CONDENSED CONSOLIDATED STATEMENTS OF CHANGES IN EQUITY
(Unaudited)
(In thousands)
Three Months Ended June 30, 2023 and 2022
Common Stock
Additional Paid-In Capital
Accumulated Deficit
Non-controlling Interest
Total Equity
Shares
Par Value
Balance at March 31, 2022
34,453
$
34
$
68,023
$
(
18,496
)
$
282
$
49,843
Shares issued on stock options exercises for cash
20
—
56
—
—
56
Stock based compensation
—
—
1,714
—
—
1,714
Shares issued on net settlement of stock options
20
—
—
—
—
—
Net loss
—
—
—
(
5,426
)
(
24
)
(
5,450
)
Balance at June 30, 2022
34,493
$
34
$
69,793
$
(
23,922
)
$
258
$
46,163
Balance at March 31, 2023
34,598
$
35
$
75,235
$
(
39,218
)
$
162
$
36,214
Shares issued on stock options exercises for cash
25
—
56
—
—
56
Stock based compensation
—
—
1,482
—
—
1,482
Shares issued on net settlement of stock options
6
—
—
—
—
—
Net loss
—
—
—
(
994
)
(
25
)
(
1,019
)
Balance at June 30, 2023
34,629
$
35
$
76,773
$
(
40,212
)
$
137
$
36,733
Six Months Ended June 30, 2023 and 2022
Common Stock
Additional Paid-In Capital
Accumulated Deficit
Non-controlling Interest
Total
Shares
Par Value
Balance at December 31, 2021
34,410
$
34
$
66,221
$
(
12,551
)
$
305
$
54,009
Shares issued on stock options exercises for cash
44
—
208
—
—
208
Stock based compensation
—
—
3,364
—
—
3,364
Shares issued on net settlement of stock options
39
—
—
—
—
—
Net loss
—
—
—
(
11,371
)
(
47
)
(
11,418
)
Balance at June 30, 2022
34,493
$
34
$
69,793
$
(
23,922
)
$
258
$
46,163
Balance at December 31, 2022
34,598
$
35
$
73,282
$
(
35,735
)
$
211
$
37,793
Shares issued on stock options exercises for cash
25
—
56
—
—
56
Stock based compensation
—
—
2,849
—
—
2,849
Shares issued on net settlement of stock options
6
—
—
—
—
—
Proceeds received from issuance of warrants
—
—
586
—
—
586
Net loss
—
—
—
(
4,477
)
(
74
)
(
4,551
)
Balance at June 30, 2023
34,629
$
35
$
76,773
$
(
40,212
)
$
137
$
36,733
The accompanying notes are an integral part of the condensed consolidated financial statements.
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APYX MEDICAL CORPORATION
CONDENSED CONSOLIDATED STATEMENTS OF CASH FLOWS
(Unaudited)
(In thousands)
Six Months Ended June 30,
2023
2022
Cash flows from operating activities
Net loss
$
(
4,551
)
$
(
11,418
)
Adjustments to reconcile net loss to net cash used in operating activities:
Depreciation and amortization
354
472
Provision for inventory obsolescence
178
139
(Gain) loss on disposal of property and equipment
(
2,692
)
47
Stock based compensation
2,849
3,364
Provision for allowance for doubtful accounts
55
284
Non-cash interest expense
209
—
Non-cash lease expense
22
—
Changes in operating assets and liabilities:
Trade receivables
(
1,441
)
2,236
Prepaid expenses and other assets
(
57
)
(
549
)
Income tax receivables
(
207
)
—
Inventories
534
(
3,187
)
Accounts payable
(
26
)
33
Accrued and other liabilities
(
1,960
)
(
1,811
)
Net cash used in operating activities
(
6,733
)
(
10,390
)
Cash flows from investing activities
Purchases of property and equipment
(
266
)
(
680
)
Proceeds from sale of property and equipment
7,267
—
Net cash provided by (used in) investing activities
7,001
(
680
)
Cash flows from financing activities
Proceeds from stock option exercises
56
208
Proceeds from term loan
9,289
—
Payment of debt issuance costs
(
1,754
)
—
Proceeds from issuance of warrants
586
—
Repayment of finance lease liabilities
(
19
)
(
108
)
Net cash provided by financing activities
8,158
100
Effect of exchange rates on cash
(
139
)
163
Net change in cash and cash equivalents
8,287
(
10,807
)
Cash and cash equivalents, beginning of period
10,192
30,870
Cash and cash equivalents, end of period
$
18,479
$
20,063
Cash paid for:
Interest
$
431
$
11
Income taxes
$
227
$
8
Non cash activities:
Right-of-use assets capitalized and operating lease liabilities recognized upon execution of lease
$
4,917
$
—
Right-of-use assets capitalized and operating lease liabilities recognized upon lease modification
$
—
$
600
Right-of-use assets capitalized and finance lease liabilities recognized upon execution of lease
$
—
$
103
The accompanying notes are an integral part of the condensed consolidated financial statements.
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APYX MEDICAL CORPORATION
NOTES TO CONDENSED CONSOLIDATED FINANCIAL STATEMENTS
(Unaudited)
NOTE 1.
BASIS OF PRESENTATION
Apyx Medical Corporation (“Company”, “Apyx”, “it” and similar terms) was incorporated in 1982, under the laws of the State of Delaware and has its principal executive office at 5115 Ulmerton Road, Clearwater, FL 33760.
The Company is an advanced energy technology company with a passion for elevating people’s lives through innovative products, including its Helium Plasma Technology products marketed and sold as Renuvion® in the cosmetic surgery market and J-Plasma® in the hospital surgical market. Renuvion® and J-Plasma® offer surgeons a unique ability to provide controlled heat to tissue to achieve their desired results. The Company also leverages its deep expertise and decades of experience in unique waveforms through OEM agreements with other medical device manufacturers.
As part of its plan to accelerate and fully fund the development of its advanced energy
business, with a focus in the cosmetic
surgery market, the Company sold its Core business in 2018 for gross proceeds of $
97
million.
These proceeds were used to launch broad marketing and sales initiatives which resulted in rapid sales growth through December 31, 2021 and into the first quarter of 2022.
This planned growth in the business was accompanied by scaled operations, including procurement of components, expanded manufacturing capacity to turn those materials into saleable inventory, additional discretionary expenditures, including increased global participation at trade shows, additional employee trainings, user meetings, increased travel and entertainment expenses, more expansive research and development projects, and additional headcount to support those activities. Additionally, the Company had, and still has, some significant non-recurring discretionary expenditures associated with completing its multi-year marketing initiatives related to its dermal resurfacing and skin laxity clearances.
On March 14, 2022, the U.S. Food and Drug Administration (“FDA”) posted a Medical Device Safety Communication (“Safety Communication”). The FDA warned against the use of Renuvion/J-Plasma for procedures intended to improve the appearance of the skin through dermal resurfacing (a procedure on the skin to treat wrinkles) or skin contraction (a procedure under the skin that can be performed either alone or in combination with liposuction to achieve skin effects, such as “tightening”). At that time, the Renuvion/J-Plasma device system was FDA cleared for general use of cutting, coagulation, and ablation of soft tissue during open and laparoscopic surgical procedures. The use of the device had not been determined to be safe or effective for any aesthetic skin procedures (procedures intended to improve the appearance of the skin). Following the Safety Communication, the Company experienced slowed demand for the adoption of its Helium Plasma Technology.
On May 26, 2022, the Company announced that it received 510(k) clearance from the FDA for the use of the Renuvion® Dermal Handpiece for certain dermal resurfacing procedures, specifically, for the treatment of moderate to severe wrinkles and rhytides, limited to patients with Fitzpatrick Skin Types I, II or III.
On June 2, 2022, the FDA updated the Safety Communication to inform consumers and healthcare providers about the new 510(k) clearance for the Renuvion® device system for certain dermal resurfacing procedures.
On July 18, 2022, the Company announced that it received 510(k) clearance from the FDA for the use of the Renuvion® APR Handpiece for use in subcutaneous dermatological and aesthetic procedures to improve the appearance of lax (loose) skin in the neck and submental (under the chin) region.
On July 21, 2022, the FDA updated the Safety Communication to inform consumers and healthcare providers about the clearance for the Renuvion® APR handpieces for use under the skin in certain procedures intended to improve the appearance of loose skin.
On February 27, 2023, the Company announced that it received 510(k) clearance from the FDA for the use of the Renuvion® APR Handpiece for the delivery of radiofrequency energy and/or helium plasma where coagulation/contraction of soft tissue is needed. Soft tissue includes subcutaneous tissue.
On April 28, 2023, the Company announced that it received 510(k) clearance from the FDA for the use of the Renuvion® APR Handpiece for coagulation of subcutaneous soft tissues following liposuction for aesthetic body contouring.
On May 10, 2023, the FDA updated the Safety Communication to inform consumers and healthcare providers about the clearance for the Renuvion® APR handpiece for use under the skin in certain procedures intended to improve the appearance of the skin, including for coagulation of subcutaneous soft tissues following liposuction for aesthetic body contouring.
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APYX MEDICAL CORPORATION
NOTES TO CONDENSED CONSOLIDATED FINANCIAL STATEMENTS - Continued
(Unaudited)
Management believes that the May 10, 2023 FDA update to the Safety Communication addresses the issues set forth in the original Safety Communication from March 14, 2022. While no assurances can be provided, management believes that receiving these additional clearances and the corresponding updates to the Safety Communication since March 14, 2022 should assist in mitigating the financial effects of the Safety Communication in future periods.
The accompanying unaudited condensed consolidated financial statements have been prepared assuming the Company will continue as a going concern. The going concern basis of presentation assumes that the Company will continue in operation one year after the date these financial statements are issued and will be able to realize its assets and discharge its liabilities and commitments in the normal course of business.
Pursuant to the requirements of the Financial Accounting Standards Board’s Accounting Standards Codification (“ASC”) Topic 205-40,
Disclosure of Uncertainties about an Entity’s Ability to Continue as a Going Concern
, management must evaluate whether there are conditions or events, considered in the aggregate, that raise substantial doubt about the Company’s ability to continue as a going concern for one year from the date these unaudited condensed consolidated financial statements are issued. This evaluation does not take into consideration the potential mitigating effect of management’s plans that have not been fully implemented or are not within control of the Company as of the date the unaudited condensed consolidated financial statements are issued. When substantial doubt exists under this methodology, management evaluates whether the mitigating effect of its plans sufficiently alleviates substantial doubt about the Company’s ability to continue as a going concern. The mitigating effect of management’s plans, however, is only considered if both (1) it is probable that the plans will be effectively implemented within one year after the date that the financial statements are issued, and (2) it is probable that the plans, when implemented, will mitigate the relevant conditions or events that raise substantial doubt about the entity’s ability to continue as a going concern within one year after the date that the financial statements are issued.
While sales were continuing to grow into the first quarter of 2022 prior to the FDA Safety Communication, over the last few years, exclusive of the Company’s sale of the Core business segment to Symmetry Surgical during 2018, the Company has incurred recurring net losses and cash outflows from operations and the Company anticipates that losses will continue in the near term. During the year ended December 31, 2022, the Company incurred an operating loss of $
23.6
million and used $
20.3
million of cash in operations. During the six months ended June 30, 2023, the Company incurred an operating loss of $
6.8
million and used $
6.7
million of cash in operations. As of June 30, 2023, the Company had cash and cash equivalents of $
18.5
million, of which the Company must maintain $
10.0
million under its Credit Agreement. These conditions raise substantial doubt about the Company’s ability to continue as a going concern for a period of at least one year from the date of issuance of these unaudited condensed consolidated financial statements.
In an effort to alleviate these conditions, the Company pursued various funding solutions in order to improve liquidity.
On November 22, 2022, the Company filed a shelf registration statement providing it the ability to register securities in the aggregate amount up to $
100
million. The shelf registration included an embedded ATM facility for up to $
40
million. To date, the Company has not utilized this facility.
On February 17, 2023, the Company entered into a Credit, Security and Guaranty Agreement (the “Credit Agreement”) with MidCap Funding IV Trust (as agent), and MidCap Financial Trust (as term loan servicer), and the lenders party thereto from time to time.
The Credit Agreement provides for an up to $
35
million facility, consisting of senior secured term loans and a secured revolving facility. The Credit Agreement provides for senior secured term loans of up to $
25
million, comprised of (i) an initial tranche of $
10
million, (ii) a second tranche of $
5
million, and (iii) a third tranche of $
10
million. The secured revolving facility provides for loans in an aggregate principal amount of up to $
10
million, subject to a borrowing base equal to certain percentages of the Company’s eligible accounts receivable and inventory, as determined in accordance with the terms of the Credit Agreement.
For a more in depth description of the terms of the Credit Agreement, see Note 7.
On February 27, 2023, the Company’s Board of Directors approved a plan to sell and leaseback the Company’s real property located in Clearwater, FL. On March 14, 2023, the Company entered into a Purchase and Sale Agreement (the “Purchase Agreement”) with VK Acquisitions VI, LLC (the “Purchaser”), for the sale of the Company’s facility located at 5115 Ulmerton Road, Clearwater, Florida, as more fully described in the Purchase Agreement (collectively, the “Property”) for a purchase price
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APYX MEDICAL CORPORATION
NOTES TO CONDENSED CONSOLIDATED FINANCIAL STATEMENTS - Continued
(Unaudited)
of $
7,650,000
. On May 8, 2023, the Company closed on the Purchase Agreement and concurrently executed a
10-year
agreement to leaseback the underlying Property from the Purchaser.
For a more in depth description of the terms of the Purchase Agreement, see Notes 4 and 5.
During January 2023, the Company was notified that the IRS examination process of our 2018, 2019 and 2020 tax returns was complete and that the Company’s tax refunds were approved for approximately $
0.2
million more than the amount recorded in the Company’s Consolidated Balance Sheet at December 31, 2022. On August 10, 2023, the Company received $
8.1
million from the IRS, which included approximately $
0.4
million of interest on the $
7.7
million income tax refunds.
The Company also re-assessed its operating expenditures and cost structure and made adjustments in light of expected levels of revenue. This included reducing some operating expenditures, including a reduction-in-force on January 9, 2023, that reduced the Company’s U.S. headcount by
14
%.
Management believes that the actions already taken, and additional actions that it can take to manage operating expenditures, will enable the Company to meet its obligations and its debt covenants for a period of at least one year from the date of issuance of these unaudited condensed consolidated financial statements. As a result, management believes its plans alleviate substantial doubt about the Company’s ability to continue as a going concern. These unaudited condensed consolidated financial statements do not include any adjustments relating to the carrying amounts and classification of assets and liabilities that may be necessary should the Company be unable to continue as a going concern.
NOTE 2.
RECENT ACCOUNTING PRONOUNCEMENTS
In June 2016, the Financial Accounting Standards Board (“FASB”) issued Accounting Standards Update (“ASU”) 2016-13,
Financial Instruments—Credit Losses (Topic 326).
The update changes the impairment model for most financial assets and certain other instruments, including trade and other receivables, contract assets, held-to-maturity debt securities and loans, and requires entities to use a new forward-looking expected loss model that will result in the earlier recognition of allowance for losses. This update, as originally issued, was effective for annual and interim periods beginning after December 15, 2019, with early adoption permitted. In November 2019, the FASB issued ASU 2019-10,
Financial Instruments - Credit Losses (Topic 326), Derivatives and Hedging (Topic 815), and Leases (Topic 842) Effective Dates
, which deferred the effective dates of these standards for Smaller Reporting Companies until fiscal years beginning after December 15, 2022. The Company adopted the new standard on January 1, 2023 and its impact was not material to the Company.
No other new accounting pronouncement issued or effective during the fiscal year had or is expected to have a material impact on our consolidated financial statements or disclosures.
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APYX MEDICAL CORPORATION
NOTES TO CONDENSED CONSOLIDATED FINANCIAL STATEMENTS - Continued
(Unaudited)
NOTE 3.
INVENTORIES
Inventories are stated at the lower of cost or net realizable value. Cost is determined on a first in, first out basis. Finished goods and work-in-process inventories include material, labor and overhead costs. Factory overhead costs are primarily allocated to inventory manufactured in-house based upon direct labor hours.
Inventories consisted of the following:
(In thousands)
June 30,
2023
December 31,
2022
Raw materials
$
4,663
$
4,979
Work in process
2,559
2,160
Finished goods
4,524
5,115
Gross inventories
11,746
12,254
Less: provision for obsolescence
(
579
)
(
457
)
Inventories, net
$
11,167
$
11,797
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APYX MEDICAL CORPORATION
NOTES TO CONDENSED CONSOLIDATED FINANCIAL STATEMENTS - Continued
(Unaudited)
NOTE 4.
PROPERTY AND EQUIPMENT
(In thousands)
June 30, 2023
(Unaudited)
December 31,
2022
Land
$
—
$
1,600
Building and improvements
—
4,426
Machinery and equipment
2,555
2,613
Furniture and fixtures
222
211
Computer equipment and software
1,230
1,420
Leasehold improvements
178
178
Molds
919
847
Total property, plant and equipment
5,104
11,295
Less: accumulated depreciation and amortization
(
3,530
)
(
5,041
)
Property and equipment in service
1,574
6,254
Construction in progress
544
507
Property and equipment, net
$
2,118
$
6,761
In an effort to improve liquidity and the balance sheet condition of the Company, management explored options to leverage the Company’s unencumbered real property. On February 27, 2023, the Company’s Board of Directors approved a plan to sell and leaseback the Company's real property located in Clearwater, FL.
On March 14, 2023, the Company entered into a Purchase and Sale Agreement (the “Purchase Agreement”) with VK Acquisitions VI, LLC (the “Purchaser”), for the sale of the Company’s facility located at 5115 Ulmerton Road, Clearwater, Florida, as more fully described in the Purchase Agreement (collectively, the “Property”) for a purchase price of $
7,650,000
.
On May 8, 2023, the Company closed on the Purchase Agreement and concurrently executed a
10-year
agreement to leaseback the underlying Property from the Purchaser (see Note 5). The Company received net cash proceeds of approximately $
6,600,000
, after withholding the security deposit of approximately $
0.6
million, equal to
one year
's rent, taxes, first months rent, expenses, and fees. The $
2,700,000
gain on this transaction is presented in gain on sale-leaseback in the accompanying Condensed Consolidated Statements of Operations for the three and six months ended June 30, 2023.
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APYX MEDICAL CORPORATION
NOTES TO CONDENSED CONSOLIDATED FINANCIAL STATEMENTS - Continued
(Unaudited)
NOTE 5.
LEASES
Operating Leases
The Company leases its facility in Sofia, Bulgaria and computers under non-cancelable operating lease agreements. These operating leases have terms expiring through December 2027.
In connection with the terms of the Purchase Agreement (see Note 4), during May 2023, the Company entered into a Single Tenant Industrial Building Lease (the “Lease”), pursuant to which the Property was leased back to the Company. The Lease has an initial term of ten (
10
) years commencing from the closing (the “Initial Term”), and a renewal term of five (
5
) years, exercisable at the Company’s option. The annual fixed rent is $
619,500
for the first year of the Initial Term, and is subject to a
4
% escalation every year thereafter through the Initial Term. Rent will be reset to the current market rate should the Company exercise the renewal option. The Lease provides for a
3
% management fee on rent payments throughout the Initial Term and optional renewal term.
The Lease is a triple net lease, pursuant to which all costs, expenses, and obligations relating to the Property, including, repair and maintenance charges, utility charges, real estate taxes or other taxes that may be imposed that relate to the Property, shall be paid by the Company. In addition, the Lease contains other customary terms and provisions generally contained within leases of this type.
Information about the Company’s weighted average remaining operating lease terms and discount rate assumptions are as follows:
June 30, 2023
December 31, 2022
Weighted average remaining lease term (in years)
9.3
4.4
Weighted average discount rate
8.36
%
2.54
%
Maturities of operating lease liabilities as of June 30, 2023 are as follows:
(In thousands)
2023
$
417
2024
777
2025
803
2026
830
2027
858
Thereafter
4,516
Total lease payments
8,201
Less imputed interest
(
2,771
)
Present value of lease liabilities
5,430
Less current portion of lease liabilities
(
337
)
Long-term portion of lease liabilities
$
5,093
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APYX MEDICAL CORPORATION
NOTES TO CONDENSED CONSOLIDATED FINANCIAL STATEMENTS - Continued
(Unaudited)
NOTE 6.
ACCRUED EXPENSES AND OTHER CURRENT LIABILITIES
Accrued expenses and other current liabilities consisted of the following:
(in thousands)
June 30,
2023
December 31,
2022
Accrued payroll
$
636
$
563
Accrued bonuses
1,029
—
Accrued commissions
1,227
847
Accrued product warranties
387
391
Accrued product liability claim insurance deductibles
1,808
1,825
Accrued professional fees and legal related contingent liabilities
639
901
Joint and several payroll liability
—
345
Short-term contract liabilities
442
853
Uncertain tax positions
—
2,079
Sales tax payable
241
245
Other accrued expenses and current liabilities
705
879
Total accrued expenses and other current liabilities
$
7,114
$
8,928
During April 2023, the Company was relieved of the remainder of its joint and several payroll liability due to the lapse of the statute of limitations. This adjustment is included in other income, net for the three and six months ended June 30, 2023.
12
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APYX MEDICAL CORPORATION
NOTES TO CONDENSED CONSOLIDATED FINANCIAL STATEMENTS - Continued
(Unaudited)
NOTE 7.
CREDIT AGREEMENT
On February 17, 2023, the Company entered into a Credit, Security and Guaranty Agreement (the “Credit Agreement”), by and among the Company (as borrower) and Apyx China Holding Corp., the Company’s wholly-owned subsidiary (as guarantor), and MidCap Funding IV Trust (as agent), and MidCap Financial Trust (as term loan servicer), and the lenders party thereto from time to time (collectively “MidCap”).
The Credit Agreement provides for an up to $
35
million facility, consisting of senior secured term loans and a secured revolving facility. The Credit Agreement provides for senior secured term loans of up to $
25
million, comprised of (i) an initial tranche of $
10
million, (ii) a second tranche of $
5
million, and (iii) a third tranche of $
10
million. The secured revolving facility provides for loans in an aggregate principal amount of up to $
10
million, subject to a borrowing base equal to percentages of eligible accounts receivable and inventory determined in accordance with the Credit Agreement. The Credit Agreement matures on February 1, 2028.
Term Loans
The initial tranche of $
10
million was fully funded on February 17, 2023 less transaction costs. Subject to certain terms and conditions of the Credit Agreement, the second tranche would be available between June 30, 2023 and December 31, 2023 and the third tranche would be available between January 1, 2024 and September 30, 2024, respectively. The Company’s ability to access these additional tranches is conditioned upon, among other things, the achievement of certain minimum revenue targets.
Each term loan bears interest at a floating rate reset monthly based on an adjusted one month SOFR plus
0.1
%, subject to a floor of
2.5
%, plus
7.35
% calculated on a 360 day basis (
12.6
% at June 30, 2023). Interest is payable monthly in arrears on the first day of each month.
The first twenty-four (
24
) months of the term loans constitute an interest-only period (with a possible twelve (
12
) month extension). Subsequent to the interest-only period, the outstanding principal amount of the term loans is repayable in thirty-six (
36
) equal monthly payments (or twenty-four (
24
) with the extension). All remaining outstanding principal, together with all accrued and unpaid interest, is due at maturity on February 1, 2028. The term loans may be voluntarily prepaid in full, or in part, at any time, subject to terms and conditions set forth in the Credit Agreement. Additionally, the term loans are subject to mandatory prepayment fees, pursuant to the terms of the Credit Agreement. Prepayments of the term loans are subject to fees of
3
%,
2
%, and
1
% of the prepayment amounts made during the first year, second year, and thereafter, respectively. At the time of the final payment of the term loans, the Company is also obligated to pay an exit fee of
4
% of the total amount funded thereunder. The exit fee is being accreted over the life of the Credit Agreement utilizing the effective interest method.
As the Credit Agreement contains a subjective acceleration clause and the Company has experienced recurring losses, outstanding borrowings have been presented as a current liability in the accompanying condensed consolidated balance sheet at June 30, 2023.
Revolving Facility
The Company may borrow, repay and reborrow under the revolving facility until February 1, 2028, at which time the facility will terminate and all outstanding amounts thereunder, including all accrued and unpaid interest, must be repaid. Borrowings are limited to the lesser of the Company’s borrowing base and the revolving commitment of $
10,000,000
.
In connection with the revolving facility, the Company is required to maintain a lockbox account for the benefit of MidCap. Funds deposited into the lockbox account will be swept daily to MidCap and applied to outstanding borrowings under the revolving agreement
5
days after the receipt of the funds by MidCap. Any balances in excess of the revolving borrowings will be promptly returned to the Company.
Loans made under the revolving facility bear interest at a floating rate based on an adjusted one month SOFR plus
0.1
%, subject to a floor of
2.5
%, plus
4.00
% calculated on a 360 day basis (
9.3
% at June 30, 2023). The Company is obligated to pay a fee equal to
0.5
% per annum on the outstanding balance of the revolving loans and the average unused portion of the available revolving commitments, respectively. Additionally, if the revolving facility is terminated or reduced before maturity, the Company is subject to a deferred origination fee. Terminations and reductions of the commitments are subject to fees of
3
%,
2
%, and
1
% of the terminated or reduced commitments during the first year, second year, and thereafter, respectively. The Company is also required to maintain a minimum balance of
30
% of the lesser of the borrowing base or $
10
million under the revolving facility. If the average outstanding balance for a month is less than the minimum balance, the Company will pay a minimum balance fee for the difference between the minimum balance and the average outstanding balance for the month at the
13
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APYX MEDICAL CORPORATION
NOTES TO CONDENSED CONSOLIDATED FINANCIAL STATEMENTS - Continued
(Unaudited)
highest rate for the revolving loans during the month. For such loans, interest and fees are payable monthly on the first day of each month.
As of June 30, 2023, the Company has drawn no amounts on the revolving facility. As of June 30, 2023, the Company had approximately $
8,000,000
available to be drawn on the revolving facility. As the Credit Agreement contains a subjective acceleration clause and the Company is required to maintain a lockbox, any amounts drawn on the revolving facility will be presented as a current liability in the consolidated financial statements.
Collateral
The obligations of the Company under the Credit Agreement are secured by first priority liens on substantially all of its assets.
Covenants
The Credit Agreement contains customary affirmative and negative covenants, including covenants limiting the ability of the Company and its subsidiaries, among other things, to incur debt, grant liens, make distributions, enter certain restrictive agreements, pay or modify subordinated debt, dispose of assets, make investments and acquisitions, enter into certain transactions with affiliates, and undergo certain fundamental changes, in each case, subject to limitations and exceptions.
The Credit Agreement also requires the Company to satisfy certain financial covenants, including minimum trailing twelve (12) month net revenue targets relating to its Advanced Energy segment (tested quarterly), with year-end targets of $
49
million, $
60
million and $
70
million for 2023, 2024, and 2025, respectively. Additionally, the Company must maintain a balance of $
10
million in cash and cash equivalents during the duration of the Credit Agreement’s term.
As of June 30, 2023, the Company was in compliance with the financial covenants contained within the Credit Agreement.
Events of Default
The Credit Agreement also contains customary Events of Default
that include, among other things, certain payment defaults, cross defaults to certain other contracts and indebtedness, covenant defaults, inaccuracy of representations and warranties, bankruptcy and insolvency defaults, judgment defaults, change of control defaults, defaults related to the failure to remain registered with the Securities and Exchange Commission and listed for trading on the Nasdaq Stock Market, and any material adverse change.
Upon the occurrence and during the continuance of an Event of Default under the Credit Agreement, the respective administrative agent, if requested by the respective lenders, may, among other things, (i) suspend or terminate commitments, as well as obligations of the relevant administrative agent and lenders, (ii) declare all outstanding obligations under the agreement (including principal and accrued and unpaid interest) immediately due and payable, and (iii) exercise the other rights and remedies provided for under the agreement. The Credit Agreement provides that, under certain circumstances, a default interest rate will apply on all obligations under such agreement during the existence of an Event of Default, at a per annum rate equal to
2
% in excess of the applicable interest rate.
The Company bifurcated a derivative liability related to the potential acceleration triggered upon an event of default (contingent put option) and the supplemental interest upon an event of default features of the Credit Agreement. The bifurcated derivative is de minimis to the Company's unaudited condensed consolidated financial statements.
Issuance of Warrants
In connection with the Company’s obligations under the Credit Agreement, the Company issued to a statutory trust of MidCap Financial warrants to purchase up to
250,000
shares of its common stock, par value $
0.001
, with an exercise price of $
3.40
per share.
The warrants have a
10
year term and can be exercised by issuing payment to the Company for the number of warrants exercised or exercised net by surrendering warrants with an intrinsic value equal to the cumulative exercise price of the warrants being exercised.
The Company determined that these warrants meet the criteria for equity classification and included the proceeds allocated to the warrants, on a relative fair value basis, as a debt discount and additional paid-in capital in the accompanying condensed consolidated financial statements.
14
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APYX MEDICAL CORPORATION
NOTES TO CONDENSED CONSOLIDATED FINANCIAL STATEMENTS - Continued
(Unaudited)
Debt Issuance Costs
In connection with entering into the Credit Agreement, the Company incurred debt issuance costs of approximately $
1.8
million, comprised primarily of commissions paid to the financial advisor. These costs were allocated to the issued and unissued term loans and the revolving facility. The costs allocated to the issued term loan will be amortized using the effective interest method over the life of the loan. The costs allocated to the unissued term loans have been deferred and will be amortized over the life of the term loans starting at the issuance date. If these loans are not issued, the Company will recognize the deferred costs at the point that the Company's rights to borrow on the term loans expires. The costs allocated to the revolving facility will be recognized on a straight-line basis over the term of the Credit Agreement.
The costs allocated to the issued term loan have been presented as a reduction of the term loan in the accompanying unaudited condensed consolidated balance sheet. The costs allocated to the unissued term loans and the revolving facility have been presented in prepaid expenses and other current assets in the accompanying unaudited condensed consolidated balance sheet.
Included in interest expense for the three and six months ended June 30, 2023 are $
35,000
and $
51,000
, respectively, of amortization of the debt issuance costs and $
80,000
and $
117,000
, respectively, of amortization of the debt discounts including accretion of the exit fee on the term loan. Included in interest expense for the three and six months ended June 30, 2023 are $
25,000
and $
37,000
, respectively, of amortization of the debt issuance costs and $
3,000
and $
4,000
, respectively, of amortization of the debt discount on the revolving facility.
The Company’s term loan, net consists of the following at June 30, 2023:
(In thousands)
June 30, 2023
Term loan
$
10,000
Unamortized debt issuance costs
(
450
)
Unamortized debt discount, including accretion of exit fee
(
658
)
Term loan, net
$
8,892
As of June 30, 2023, principal repayments on the term loan are as follows:
(In thousands)
2023
$
—
2024
—
2025
2,778
2026
3,333
2027
3,333
Thereafter
556
Total repayments
$
10,000
15
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APYX MEDICAL CORPORATION
NOTES TO CONDENSED CONSOLIDATED FINANCIAL STATEMENTS - Continued
(Unaudited)
NOTE 8.
CHINA JOINT VENTURE
In 2019, the Company executed a joint venture agreement with its Chinese supplier (the “China JV”) whereby the Company has a
51
% interest. The China JV has been consolidated in these condensed consolidated financial statements. The agreement required the Company to make capital contributions into the newly formed entity of approximately $
357,000
, of which approximately $
203,000
and $
154,000
, respectively, were contributed during the years ended December 31, 2021 and 2020. In June 2023, the Company executed an amendment to the joint venture agreement to increase the amount of it’s registered capital. The amendment requires the Company to make additional capital contributions to the China JV of $
255,000
, which have not been made as of June 30, 2023. As of the date of these condensed consolidated financial statements, the joint venture has not commenced principal operations.
Changes in the
Company
’
s ownership
investment in the China JV were as follows:
Three Months Ended June 30,
Six Months Ended
June 30,
(In thousands)
2023
2022
2023
2022
Beginning interest in China JV
$
168
$
294
$
219
$
317
Net loss attributable to Apyx
$
(
26
)
$
(
25
)
$
(
77
)
$
(
48
)
Ending interest in China JV
$
142
$
269
$
142
$
269
NOTE 9.
EARNINGS (LOSS) PER SHARE
Basic earnings (loss) per share (“basic EPS”) is computed by dividing the net income or loss by the weighted average number of common shares outstanding for the reporting period. Diluted earnings (loss) per share (“diluted EPS”) gives effect to all dilutive potential shares outstanding. As the Company is in a net loss position for all periods presented, all potential shares outstanding are anti-dilutive.
The following table provides the computation of basic and diluted loss per share.
Three Months Ended
June 30,
Six Months Ended
June 30,
(in thousands, except per share data)
2023
2022
2023
2022
Numerator:
Net loss attributable to stockholders
$
(
994
)
$
(
5,426
)
$
(
4,477
)
$
(
11,371
)
Denominator:
Weighted average shares outstanding - basic and diluted
34,603
34,464
34,600
34,447
Loss per share:
Basic and diluted
$
(
0.03
)
$
(
0.16
)
$
(
0.13
)
$
(
0.33
)
Anti-dilutive instruments excluded from diluted loss per common share:
Options
7,700
6,679
7,700
6,679
Warrants
250
—
250
—
16
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APYX MEDICAL CORPORATION
NOTES TO CONDENSED CONSOLIDATED FINANCIAL STATEMENTS - Continued
(Unaudited)
NOTE 10.
STOCK-BASED COMPENSATION
Under the Company’s stock option plans, the Board of Directors may grant restricted stock and options to purchase common shares to the Company's employees, officers, directors and consultants. The Company accounts for stock options in accordance with FASB ASC Topic 718,
Compensation - Stock Compensation
, with stock-based compensation expense recognized over the vesting period based on the fair value on the grant date utilizing the Black-Scholes model, which includes a number of estimates that affect the grant date fair value and the amount of expense to recognize.
The Company recognized approximately $
1,482,000
and $
2,849,000
, respectively, in stock-based compensation expense during the three and six months ended June 30, 2023, as compared with $
1,714,000
and $
3,364,000
, respectively, for the three and six months ended June 30, 2022.
Stock option activity is summarized as follows:
Number of options
Weighted average exercise price
Outstanding at December 31, 2022
6,520,444
$
7.12
Granted
1,408,865
2.50
Exercised
(
35,000
)
2.46
Canceled and forfeited
(
194,225
)
8.11
Outstanding at June 30, 2023
7,700,084
$
6.27
The Company allows stock option holders to exercise stock-based awards by surrendering stock-based awards with an intrinsic value equal to the cumulative exercise price of the stock-based awards being exercised, referred to as net settlements. These surrenders are included in stock options exercised in the options rollforward above. For the three months ended June 30, 2023 and 2022, respectively, we received
4,305
and
14,013
options as payment in the exercise of
5,695
and
19,987
options. For the six months ended June 30, 2023 and 2022, respectively, we received
4,305
and
36,667
options as payment in the exercise of
5,695
and
39,000
options.
Common shares required to be issued upon the exercise of stock options would be issued from authorized and unissued shares.
The Company calculated the grant date fair value of options granted in 2023 (“2023 Grants”) utilizing a Black-Scholes model.
2023 Grants
Strike price
$
2.50
Risk-free rate
3.6
%
Expected dividend yield
—
Expected volatility
85.8
%
Expected term (in years)
6
NOTE 11.
INCOME TAXES
Income tax expense was approximately $
66,000
and $
96,000
with effective tax rates of (
6.9
)% and (
1.8
)% for the three months ended June 30, 2023 and 2022, respectively. For the three months ended June 30, 2023 and 2022, the effective rates differ from the statutory rate primarily due to the full valuation allowance recorded on the net operating loss (“NOL”) generated during the period.
Income tax (benefit) expense was approximately $(
2,201,000
) and $
166,000
with effective tax rates of
32.6
% and (
1.5
)% for the six months ended June 30, 2023 and 2022, respectively. For the six months ended June 30, 2023, the effective rate differs from the statutory rate primarily due to the reversal of the Company’s liability for uncertain tax positions, including accrued interest and penalties of approximately $
2.1
million which were sustained upon the completion in January 2023 of the IRS examination of the Company's 2018 through 2020 income tax returns, partially offset by a valuation allowance on the NOL and net deferred tax assets generated during the period. For the six months ended June 30, 2022, the effective rate differs from the
17
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APYX MEDICAL CORPORATION
NOTES TO CONDENSED CONSOLIDATED FINANCIAL STATEMENTS - Continued
(Unaudited)
statutory rate primarily due to the full valuation allowance recorded on the NOL generated during the period, combined with interest and penalties on uncertain tax positions.
NOTE 12.
COMMITMENTS AND CONTINGENCIES
Litigation
The medical device industry is characterized by frequent claims and litigation, and the Company may become subject to various claims, lawsuits and proceedings in the ordinary course of our business. Such claims may include claims by current or former employees, distributors and competitors, claims concerning the marketing and promotion of our products and product liability claims.
The Company is involved in a number of legal actions relating to the use of our Helium Plasma technology. The outcomes of these legal actions are not within the Company’s control and may not be known for prolonged periods of time. It believes that such claims are adequately covered by insurance; however, in the case of one of the Company’s carriers, the Company is in a dispute regarding the total level of coverage available. Notwithstanding the foregoing, in the opinion of management, the Company has meritorious defenses, and such claims are not expected, individually or in the aggregate, to result in a material, adverse effect on its financial condition, results of operations and cash flows. However, in the event that damages exceed the aggregate coverage limits of the Company’s policies or if its insurance carriers disclaim coverage, management believes it is possible that costs associated with these claims could have a material adverse impact on the consolidated financial condition, results of operations and cash flows.
During December 2021, the Company provided notice of contract termination to an international distributor of the Company. In March 2022, the Company received a letter from the former distributor citing improper contract termination and alleging damages. During 2022, the Company recorded an estimated loss of $
250,000
in professional services in the accompanying Condensed Consolidated Statement of Operations for the six months ended June 30, 2022. The Company has not experienced any movement on the matter since our response to the distributor in the fourth quarter of 2022. Accordingly, we have revised our estimated loss on the matter to $
0
as it is no longer probable that a loss has been incurred. The reduction in estimated loss of $
250,000
is included in professional services in the accompanying Condensed Consolidated Statements of Operations for the three and six months ended June 30, 2023.
As previously disclosed with the U.S. Securities and Exchange Commission on the Company’s Current Report on Form 8-K filed June 7, 2022, on June 6, 2022, a complaint (the “Hattaway Complaint”) was filed in the United States District Court for the Middle District of Florida (the “U.S. District Court”) by plaintiff William E. Hattaway, individually and on behalf of all others similarly situated against the Company, Charles D. Goodwin (“Goodwin”), the Company’s President and Chief Executive Officer and a member of the Company’s Board of Directors, and Tara Semb (“Semb”), the Company’s Chief Financial Officer, Treasurer and Secretary, alleging violations by the Company, Goodwin and Semb of Sections 10(b) and 20(a) of the Securities Exchange Act of 1934 and Rule 10b-5 thereunder, primarily related to certain public statements and disclosures concerning the off-label usage of certain of the Company’s Advanced Energy products and the impact such usage would have on the Company’s business, operations and prospects. The Hattaway Complaint sought an unspecified amount of damages.
While the matter was in the early stages, management had determined that a loss was probable in the estimated range of $
475,000
to $
2,500,000
. The Company recorded an estimated loss of $
475,000
in professional services in the accompanying Condensed Consolidated Statement of Operations for the three and six months ended June 30, 2022. On June 15, 2023, the U.S. District Court issued an Order dismissing the Hattaway Complaint and granting plaintiff until July 3, 2023 to file a second amended complaint, failing which the U.S. District Court would close the case. On June 27, 2023, the Plaintiff formally notified the Court that a Second Amended Complaint will not be filed and on July 17, 2023, the case was marked closed based on the Court’s June 15 dismissal order. This closed the matter for the estimated loss recorded by the Company.
During 2022, the Company was notified of certain procedures alleged to have been performed by the same physician and which are currently the subject of two related products liability cases within the courts. Subsequent to year end, the Company was notified by its insurance carriers that all or most of the ten individual plaintiff’s allegations could be subject to separate deductibles notwithstanding the commonality of each underlying occurrence. The Company has determined that a loss is probable and that a range of estimated losses is approximately $
1,450,000
to $
2,400,000
. The Company recorded an estimated
18
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APYX MEDICAL CORPORATION
NOTES TO CONDENSED CONSOLIDATED FINANCIAL STATEMENTS - Continued
(Unaudited)
loss of $
1,450,000
related to the matters during 2022. It is at least possible that a change in the actual amount of loss will occur in the near term, though management expects the actual amount of loss will be within the estimated range of losses.
On March 1, 2023, Shiva Stein as plaintiff filed a derivative complaint in the Court of Chancery of the State of Delaware, captioned Stein v. Makrides, et al., C.A. No. 2023-0239-MTZ (the “Stein Suit”) against individual members of the Company’s board of directors and naming the Company as a nominal defendant, primarily concerning the facts at issue in a previously disclosed federal securities class action lawsuit filed in 2019 and settled in 2020, captioned Pritchard v. Apyx Medical Corporation, et al., Case No. 8:19-cv-00919 (M.D. Fla.) (the “Pritchard Case”). The Stein Suit seeked unspecified damages alleged to have resulted from purported breaches of fiduciary duty, unjust enrichment and related claims based on the same set of allegedly misleading statements and material omissions described in the settled Pritchard Case, which concerned the 2018-2019 clinical study conducted by the Company to evaluate the safety and efficacy of its J-Plasma technology for dermal resurfacing. On April 3, 2023, the Company formally moved to dismiss the case as time-barred and on other legal grounds, which triggered the plaintiff’s right to file an amended complaint. On July 12, 2023, plaintiff’s counsel informed the Company’s counsel that plaintiff Stein did not intend to file an amended complaint, and on July 17, 2023 plaintiff’s counsel filed a notice of voluntary dismissal. An order of the Court dismissing the Stein Suit, with prejudice, was entered on July 20, 2023.
The Company accrues a liability in its consolidated financial statements for these actions when a loss is known or considered probable and the amount can be reasonably estimated. If the reasonable estimate of a known or probable loss is a range, and no amount within the range is a better estimate than any other, the minimum amount of the range is recorded. If a loss is reasonably possible, but not known or probable, and can be reasonably estimated, the estimated loss or range of loss is disclosed in the notes to the condensed consolidated financial statements. In most cases, significant judgment is required to estimate the amount and timing of a loss to be recorded, actual results may differ from these estimates.
Purchase Commitments
At June 30, 2023, the Company had purchase commitments totaling approximately $
3.3
million, substantially all of which is expected to be purchased within the next twelve months.
19
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APYX MEDICAL CORPORATION
NOTES TO CONDENSED CONSOLIDATED FINANCIAL STATEMENTS - Continued
(Unaudited)
NOTE 13.
RELATED PARTY TRANSACTIONS
Several relatives of Nikolay Shilev, Apyx Bulgaria’s Managing Director, are considered related parties. Teodora Shileva, Mr. Shilev’s spouse, is an employee of the Company working in the accounting department. Svetoslav Shilev, Mr. Shilev’s son, is a quality manager in the quality assurance department.
The partner in the Company's China joint venture is also a supplier to the Company. For the three months ended June 30, 2023 and 2022, the Company made purchases from this supplier of approximately $
406,000
and $
143,000
, respectively. For the
six months ended June 30, 2023
and 2022, the Company made purchases from this supplier of approximately $
451,000
and $
370,000
, respectively. At June 30, 2023 and December 31, 2022, respectively, the Company had net payables to and receivables from this supplier approximately $
155,000
and $
8,000
, respectively.
NOTE 14.
GEOGRAPHIC AND SEGMENT INFORMATION
Operating segments are aggregated into reportable segments only if they exhibit similar economic characteristics. In addition to similar economic characteristics, the Company also considers the following factors in determining the reportable segments: the nature of business activities, the management structure directly accountable to its chief operating decision maker for operating and administrative activities, availability of discrete financial information and information presented to the Board of Directors and investors. Asset information is not reviewed by the chief operating decision maker by segment and is not available by segment, accordingly, the Company has not presented a measure of assets by segment.
The Company
’
s reportable segments are disclosed as principally organized and managed as
two
operating segments: Advanced Energy and OEM.
“
Corporate & Other
”
includes certain unallocated corporate and administrative costs which were not specifically attributed to any reportable segment. The OEM segment is primarily development and manufacturing contract and product driven, all related expenses are recorded as cost of sales, therefore no segment specific operating expenses are incurred.
Summarized financial information with respect to reportable segments is as follows:
20
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APYX MEDICAL CORPORATION
NOTES TO CONDENSED CONSOLIDATED FINANCIAL STATEMENTS - Continued
(Unaudited)
Three Months Ended June 30, 2023
(In thousands)
Advanced Energy
OEM
Corporate & Other
Total
Sales
$
11,722
$
1,847
$
—
$
13,569
Income (loss) from operations
747
353
(
2,335
)
(
1,235
)
Interest income
—
—
179
179
Interest expense
—
—
(
543
)
(
543
)
Other income, net
—
—
646
646
Income tax expense
—
—
66
66
Three Months Ended June 30, 2022
(In thousands)
Advanced Energy
OEM
Corporate & Other
Total
Sales
$
8,364
$
1,928
$
—
$
10,292
(Loss) income from operations
(
1,252
)
469
(
5,193
)
(
5,976
)
Interest income
—
—
18
18
Interest expense
—
—
(
3
)
(
3
)
Other income, net
—
—
607
607
Income tax expense
—
—
96
96
Six Months Ended June 30, 2023
(In thousands)
Advanced Energy
OEM
Corporate & Other
Total
Sales
$
21,412
$
4,299
$
—
$
25,711
(Loss) income from operations
(
579
)
1,204
(
7,471
)
(
6,846
)
Interest income
—
—
230
230
Interest expense
—
—
(
777
)
(
777
)
Other income, net
—
—
641
641
Income tax benefit
—
—
(
2,201
)
(
2,201
)
21
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APYX MEDICAL CORPORATION
NOTES TO CONDENSED CONSOLIDATED FINANCIAL STATEMENTS - Continued
(Unaudited)
Six Months Ended June 30, 2022
(In thousands)
Advanced Energy
OEM
Corporate & Other
Total
Sales
$
19,178
$
3,607
$
—
$
22,785
(Loss) income from operations
(
2,591
)
786
(
10,042
)
(
11,847
)
Interest income
—
—
20
20
Interest expense
—
—
(
11
)
(
11
)
Other income, net
—
—
586
586
Income tax expense
—
—
166
166
International sales represented approximately
25.3
% and
26.1
% of total revenues for the three and six months ended June 30, 2023, respectively, as compared with approximately
22.8
% and
32.0
% of total revenues for the three and six months ended June 30, 2022, respectively.
Revenue by geographic region, based on the customer's “ship to” location on the invoice, are as follows:
Three Months Ended
June 30,
Six Months Ended
June 30,
(In thousands)
2023
2022
2023
2022
Sales by Domestic and International
Domestic
$
10,137
$
7,947
$
19,008
$
15,495
International
3,432
2,345
6,703
7,290
Total
$
13,569
$
10,292
$
25,711
$
22,785
22
Table of Contents
APYX MEDICAL CORPORATION
MANAGEMENT'S DISCUSSION AND ANALYSIS OF
FINANCIAL CONDITION AND RESULTS OF OPERATIONS
ITEM 2
.
Management’s Discussion and Analysis of Financial Condition and Results of Operations
You should read the following discussion and analysis in conjunction with our financial statements and related notes contained elsewhere in this report. This discussion contains forward-looking statements that involve risks, uncertainties and assumptions. Our actual results may differ materially from those anticipated in these forward-looking statements as a result of a variety of factors discussed in this report and those discussed in other documents we file with the SEC. In light of these risks, uncertainties and assumptions, readers are cautioned not to place undue reliance on such forward-looking statements. These forward-looking statements represent beliefs and assumptions as of the date of this report. While we may elect to update forward-looking statements and at some point in the future, we specifically disclaim any obligation to do so, even if our estimates change. Past performance does not guarantee future results.
Executive Level Overview
We are an advanced energy technology company with a passion for elevating people’s lives through innovative products, including our Helium Plasma Technology products marketed and sold as Renuvion® in the cosmetic surgery market and J-Plasma® in the hospital surgical market. Renuvion® and J-Plasma® offer surgeons a unique ability to provide controlled heat to tissue to achieve their desired results. We also leverage our deep expertise and decades of experience in unique waveforms through OEM agreements with other medical device manufacturers.
As part of our plan to accelerate and fully fund the development of our advanced energy
business, with a focus in the cosmetic
surgery market, we sold our Core business in 2018 for gross proceeds of $97 million.
These proceeds were used to launch broad marketing and sales initiatives which resulted in rapid sales growth through December 31, 2021 and into the first quarter of 2022.
This planned growth in the business was accompanied by scaled operations, including procurement of components, expanded manufacturing capacity to turn those materials into saleable inventory, additional discretionary expenditures, including increased global participation at trade shows, additional employee trainings, user meetings, increased travel and entertainment expenses, more expansive research and development projects, and additional headcount to support those activities. Additionally, we had and still have, some significant non-recurring discretionary expenditures associated with completing our multi-year marketing initiatives related to our dermal resurfacing and skin laxity clearances.
On March 14, 2022, the U.S. Food and Drug Administration (“FDA”) posted a Safety Communication that warns consumers and health care providers against the use of our Advanced Energy products outside of their FDA-cleared indications for general use in cutting, coagulation, and ablation of soft tissue during open and laparoscopic surgical procedures. Following the Safety Communication, we experienced slowed demand for the adoption of our Helium Plasma Technology.
On May 26, 2022, we announced that we received 510(k) clearance from the FDA for the use of the Renuvion Dermal Handpiece for specific dermal resurfacing procedures. On July 18, 2022, we announced that we received 510(k) clearance from the FDA for the use of the Renuvion® APR Handpiece for certain skin contraction procedures.
On June 2, 2022, and July 21, 2022, FDA updated the Medical Device Safety Communication to recognize the new 510(k) clearances for the Renuvion® Dermal handpiece, and the expanded indications for the Renuvion® APR handpieces. The 510(k) clearance for the Renuvion® Dermal handpiece allows surgeons to perform dermal resurfacing procedures for the treatment of moderate to severe wrinkles and rhytides, limited to patients with Fitzpatrick Skin Types I, II or III. The 510(k) clearance for the Renuvion® APR handpieces now addresses improving the appearance of lax (loose) skin in the neck and submental region.
On July 18, 2022, we announced that we received 510(k) clearance from the FDA for the use of the Renuvion® APR Handpiece for use in subcutaneous dermatological and aesthetic procedures to improve the appearance of lax (loose) skin in the neck and submental (under the chin) region.
On July 21, 2022, the FDA updated the Safety Communication to inform consumers and healthcare providers about the clearance for the Renuvion® APR handpieces for use under the skin in certain procedures intended to improve the appearance of loose skin.
On February 27, 2023, we announced that we received 510(k) clearance from the FDA for the use of the Renuvion® APR Handpiece for the delivery of radiofrequency energy and/or helium plasma where coagulation/contraction of soft tissue is needed. Soft tissue includes subcutaneous tissue.
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APYX MEDICAL CORPORATION
MANAGEMENT'S DISCUSSION AND ANALYSIS OF
FINANCIAL CONDITION AND RESULTS OF OPERATIONS - Continued
On April 28, 2023, we announced that we received 510(k) clearance from the FDA for the use of the Renuvion® APR Handpiece for coagulation of subcutaneous soft tissues following liposuction for aesthetic body contouring.
On May 10, 2023, the FDA updated the Safety Communication to inform consumers and healthcare providers about the clearance for the Renuvion® APR handpiece for use under the skin in certain procedures intended to improve the appearance of the skin, including for coagulation of subcutaneous soft tissues following liposuction for aesthetic body contouring.
We believe that the May 10, 2023 FDA update to the Safety Communication addresses the issues set forth in the original Safety Communication from March 14, 2022. While no assurances can be provided, we believe that receiving these additional clearances and the corresponding updates to the Safety Communication since March 14, 2022 should assist in mitigating the financial effects of the Safety Communication in future periods.
While sales were continuing to grow into the first quarter of 2022 prior to the FDA Safety Communication, over the last few years, exclusive of our sale of the Core business segment to Symmetry Surgical during 2018, we have incurred recurring net losses and cash outflows from operations and we anticipate that losses will continue in the near term. During the six months ended June 30, 2023, we incurred an operating loss of $6.8 million and used $6.7 million of cash in operations. As of June 30, 2023, we had cash and cash equivalents of $18.5 million. These conditions raise substantial doubt about our ability to continue as a going concern for a period of at least one year from the date of issuance of these unaudited condensed consolidated financial statements.
In an effort to alleviate these conditions, we pursued various funding solutions in order to improve liquidity.
On November 22, 2022, the we filed a shelf registration statement providing us the ability to register securities in the aggregate amount up to $100 million. The shelf registration included an embedded ATM facility for up to $40 million. To date, we have not utilized this facility.
On February 17, 2023, we entered into a Credit, Security and Guaranty Agreement (the “Credit Agreement”) with MidCap Funding IV Trust (as agent), and MidCap Financial Trust (as term loan servicer), and the lenders party thereto from time to time.
The Credit Agreement provides for an up to $35 million facility, consisting of senior secured term loans and a secured revolving facility. The Credit Agreement provides for senior secured term loans of up to $25 million, comprised of (i) an initial tranche of $10 million, (ii) a second tranche of $5 million, and (iii) a third tranche of $10 million. The secured revolving facility provides for loans in an aggregate principal amount of up to $10 million, subject to a borrowing base equal to certain percentages of the Company’s eligible accounts receivable and inventory, as determined in accordance with the terms of the Credit Agreement.
For a more in depth description of the terms of the Credit Agreement, see Note 7 of Notes to Condensed Consolidated Financial Statements in Item 1 of this report on Form 10-Q.
On February 27, 2023, our Board of Directors approved a plan to sell and leaseback the our real property located in Clearwater, FL. On March 14, 2023, we entered into a Purchase and Sale Agreement (the “Purchase Agreement”) with VK Acquisitions VI, LLC (the “Purchaser”), for the sale of our facility located at 5115 Ulmerton Road, Clearwater, Florida, as more fully described in the Purchase Agreement (collectively, the “Property”) for a purchase price of $7,650,000. The Purchase Agreement is subject to the satisfactory completion of due diligence by the Purchaser. On May 8, 2023, we closed on the Purchase Agreement and concurrently executed a 10-year agreement to leaseback the underlying Property from the Purchaser.
For a more in depth description of the terms of the Purchase Agreement, see Notes 4 and 5 of Notes to Condensed Consolidated Financial Statements in Item 1 of this report on Form 10-Q.
During January 2023, we were notified that the IRS examination process of our 2018, 2019 and 2020 tax returns was complete and that the our tax refunds were approved for approximately $0.2 million more than the amount recorded in the Company’s Consolidated Balance Sheet at December 31, 2022. On August 10, 2023, we received $8.1 million from the IRS, which included approximately $0.4 million of interest on the $7.7 million income tax refunds.
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APYX MEDICAL CORPORATION
MANAGEMENT'S DISCUSSION AND ANALYSIS OF
FINANCIAL CONDITION AND RESULTS OF OPERATIONS - Continued
We also reassessed our operating expenditures and cost structure and made adjustments in light of expected levels of revenue. This included reducing some operating expenditures, including a reduction-in-force on January 9, 2023, that reduced the our U.S. headcount by 14%.
We believe that the actions already taken, and additional actions that we can take to manage operating expenditures, will enable us to meet our obligations and our debt covenants for a period of at least one year from the date of issuance of our audited consolidated financial statements. As a result, we believe our plans alleviate substantial doubt about our ability to continue as a going concern. Our audited financial statements do not include any adjustments relating to the carrying amounts and classification of assets and liabilities that may be necessary should we be unable to continue as a going concern.
We continue to drive sales in our Advanced Energy business by increasing the adoption and utilization of our handpieces by surgeons in the U.S. and fulfilling demand from distributors in our international markets. Management estimates that our products have been sold in more than 60 countries. As of June 30, 2023, we had a direct sales force of 36 field-based selling professionals and utilized 3 independent sales agencies. We also had 4 sales managers. This selling organization is focused on the use of Renuvion® in the cosmetic surgery market, supported by our global medical affairs team. This global team of clinical support specialists focuses on supporting our users to ensure optimal outcomes for their patients. In addition, we have invested in training programs and marketing-related activities to support accelerated adoption of Renuvion® into physicians’ practices.
In regards to our operating segments, our results are aggregated into reportable segments only if they exhibit similar economic characteristics. In addition to similar economic characteristics, we also consider the following factors in determining the reportable segments: the nature of business activities, the management structure directly accountable to our chief operating decision maker for operating and administrative activities, availability of discrete financial information, and information presented to the Board of Directors and investors. Asset information is not reviewed by the chief operating decision maker by segment and is not available by segment and, accordingly, we have not presented a measure of assets by reportable segment.
Our reportable segments are disclosed as principally organized and managed as two operating segments: Advanced Energy and OEM. "Corporate & Other" includes certain unallocated corporate and administrative costs which are not specifically attributed to any reportable segment. The OEM segment is primarily development and manufacturing contract and product driven, and all related expenses are recorded as cost of sales, therefore no segment specific operating expenses are incurred.
In response to the global supply chain instability and inflationary cost increases, we continue to take action to minimize, as much as possible, any potential adverse impacts by working closely with our suppliers to closely monitor the availability of raw material components (i.e. semiconductors and plastics), lead times, and freight carrier availability.
We expect global supply chain instability will continue to have an impact on our business, but to date that has not been material to our financial performance. The consequences of the pandemic, global supply chain instability and inflationary cost increases and their adverse impact to the global economy, continue to evolve. Accordingly, the significance of the future impact to our business and financial statements remains subject to significant uncertainty.
We strongly encourage investors to visit our website:
www.apyxmedical.com
to view the most current news and to review our filings with the Securities and Exchange Commission.
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APYX MEDICAL CORPORATION
MANAGEMENT'S DISCUSSION AND ANALYSIS OF
FINANCIAL CONDITION AND RESULTS OF OPERATIONS - Continued
Results of Operations
Sales
Three Months Ended
June 30,
Six Months Ended
June 30,
(In thousands)
2023
2022
Change
2023
2022
Change
Sales by Reportable Segment
Advanced Energy
$
11,722
$
8,364
40.1
%
$
21,412
$
19,178
11.6
%
OEM
1,847
1,928
(4.2)
%
4,299
3,607
19.2
%
Total
$
13,569
$
10,292
31.8
%
$
25,711
$
22,785
12.8
%
(632,000)
Sales by Domestic and International
Domestic
$
10,137
$
7,947
27.6
%
$
19,008
$
15,495
22.7
%
International
3,432
2,345
46.4
%
6,703
7,290
(8.1)
%
Total
$
13,569
$
10,292
31.8
%
$
25,711
$
22,785
12.8
%
Total revenue increased by
31.8%
, or approximately $3.3 million, for the three months ended June 30, 2023 when compared with the three months ended June 30, 2022. Advanced Energy segmen
t sales increased 40.1%, or approximately
$3.4 million
, for the three
months ended June 30, 2023
when compared with the three
months ended June 30, 2022
.
The Advanced Energy sales increase is driven by domestic customers who upgraded their generator to our new Apyx One Console, which we launched in January 2023, a higher average selling price on sales of new generators due to the introduction of the Apyx One Console, and increased sales of our handpieces to domestic customers. These domestic increases were accompanied by an increase in generator sales in international markets. OEM segmen
t sales decreased 4.2%, or approximately
$0.8 million
, for the
three months ended June 30, 2023
when compared with the
three months ended June 30, 2022
. The decrease in OEM sales was due to decreases in sales volume to existing customers.
Total revenue increased by
12.8%
, or approximately $2.9 million, for the six months ended June 30, 2023 when compared with the six months ended June 30, 2022. Advanced Energy segmen
t sales increased 11.6%, or approximately
$2.2 million
, for the
six months ended June 30, 2023
when compared with the
six months ended June 30, 2022
.
The Advanced Energy sales increase is driven by domestic customers who upgraded their generator to our new Apyx One Console, which we launched in January 2023 and a higher average selling price on sales of new generators due to the introduction of the Apyx One Console. These domestic increases were partially offset by decreases in new generator sales, and demand for our handpieces, in international markets following the FDA Safety Communication on March 14, 2022. OEM segment sales increased 19.2%, or approximately $0.7 million, for the six months ended June 30, 2023 when compared with the six months ended June 30, 2022.
The increase in OEM sales was due to increases in sales volume to existing customers as well as incremental new sales upon the commencement of the supply arrangement related to the completion of the development portion of some of our OEM development agreements.
International sales represented approximately 25.3% and 26.1% of total revenues for the three and
six months ended June 30, 2023
, respectively, as compared with 22.8% and 32.0% of total revenues for the same period in the prior year. Management estimates our products have been sold in more tha
n 60 countr
ies through local dealers coordinated by sales and marketing personnel through our facilities in Clearwater, Florida and Sofia, Bulgaria.
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APYX MEDICAL CORPORATION
MANAGEMENT'S DISCUSSION AND ANALYSIS OF
FINANCIAL CONDITION AND RESULTS OF OPERATIONS - Continued
Gross Profit
Three Months Ended
June 30,
Six Months Ended
June 30,
(In thousands)
2023
2022
Change
2023
2022
Change
Cost of sales
$
4,290
$
3,378
27.0
%
$
8,859
$
7,652
15.8
%
Percentage of sales
31.6
%
32.8
%
34.5
%
33.6
%
Gross profit
$
9,279
$
6,914
34.2
%
$
16,852
$
15,133
11.4
%
Percentage of sales
68.4
%
67.2
%
65.5
%
66.4
%
Gross profit for the three months ended June 30, 2023, increased 34.2% to $9.3 million, compared to $6.9 million for the same period in the prior year. Gross margin for the three months ended June 30, 2023, was 68.4%,
compared to 67.2% for the same period in 2022. The increase in gross profit margins for the three months ended June 30, 2023 from the prior year period is primarily attributable to changes in the sales mix between our two segments, with our Advanced Energy segment comprising a higher percentage of total sales. These increases were partially offset by geographic mix within our Advanced Energy segment, with international sales comprising a higher percentage of total sales and product mix within our Advanced Energy segment.
Gross profit for the
six months ended June 30, 2023
, increased 11.4% to $16.9 million, compared to $15.1 million for the same period in the prior year. Gross margin for the
six months ended June 30, 2023, was 65.5%, compared to 66.4% for the same period in 2022. The decrease in gross profit margins for the six months ended June 30, 2023 from the prior year periods is primarily attributable to changes in the sales mix between our two segments, with our OEM segment comprising a higher percentage of total sales and product mix within our Advanced Energy Segment. These decreases were partially offset by geographic mix within our Advanced Energy segment, with domestic sales comprising a higher percentage of total sales.
Other Costs and Expenses
Research and development
Three Months Ended
June 30,
Six Months Ended
June 30,
(In thousands)
2023
2022
Change
2023
2022
Change
Research and development expense
$
1,199
$
1,070
12.1
%
$
2,320
$
2,228
4.1
%
Percentage of sales
8.8
%
10.4
%
9.0
%
9.8
%
Research and development expenses increased 12.1% for the three months ended June 30, 2023, primarily due to higher spending on our product development initiatives and clinical studies ($0.1 million).
Research and development expenses increased 4.1% for the six months ended June 30, 2023, primarily due to increased labor and benefits costs from the same period prior year ($0.1 million).
Professional services
Three Months Ended
June 30,
Six Months Ended
June 30,
(In thousands)
2023
2022
Change
2023
2022
Change
Professional services expense
$
1,594
$
2,389
(33.3)
%
$
3,334
$
4,675
(28.7)
%
Percentage of sales
11.7
%
23.2
%
13.0
%
20.5
%
Professional services expense decreased 33.3% for the three months ended June 30, 2023, primarily attributable to decreases in legal expenses ($0.7 million) associated with the estimated loss recorded in the prior year for the class action lawsuit and current year reversal of a legal loss contingency, and a decrease in recruiting expenses ($0.1 million).
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APYX MEDICAL CORPORATION
MANAGEMENT'S DISCUSSION AND ANALYSIS OF
FINANCIAL CONDITION AND RESULTS OF OPERATIONS - Continued
Professional ser
vices expense decreased
28.7% for the six months ended June 30, 2023, primarily attributable to decreases in legal expenses ($1.0 million) associated with the estimated loss recorded in the prior year for the class action lawsuit and current year reversal of a legal loss contingency, a
ccounting and audit fees ($0.1 million), physician consulting fees ($0.1 million),
and a decrease in recruiting expenses ($0.1 million).
Salaries and related costs
Three Months Ended
June 30,
Six Months Ended
June 30,
(In thousands)
2023
2022
Change
2023
2022
Change
Salaries and related expenses
$
5,035
$
4,892
2.9
%
$
10,103
$
10,073
0.3
%
Percentage of sales
37.1
%
47.5
%
39.3
%
44.2
%
Durin
g the three months ended June 30, 2023, salaries and related expenses increased 2.9%, primarily driven by increases in bonus expense ($0.2 million) and temporary labor expenses ($0.2 million). These increases were partially offset by lower stock based compensation expense ($0.3 million).
During the six months ended June 30, 2023, salaries and related expenses increased 0.3%, primarily driven by increases in bonus expense ($0.2 million) and temporary labor expenses ($0.3 million) as compared to the same period in the prior year. These increases are partially offset by lower stock based compensation expense ($0.5 million).
Selling, general and administrative expenses
Three Months Ended
June 30,
Six Months Ended
June 30,
(In thousands)
2023
2022
Change
2023
2022
Change
SG&A expense
$
5,378
$
4,539
18.5
%
$
10,633
$
10,004
6.3
%
Percentage of sales
39.6
%
44.1
%
41.4
%
43.9
%
During the three months ended June 30, 2023, selling, general and administrative expense increased 18.5%, primarily driven by increases in commissions ($0.4 million), insurance expense, including product liability claims on our policies ($0.2 million), advertising expense, including trade show fees and related costs ($0.1 million) and bad debt expense ($0.1 million).
During the
six months ended June 30, 2023
, selling, general and admi
nistrative expense increased 6.3%, primarily driven by increases in insurance expense, including product liability claims on our policies ($0.4 million), commissions ($0.4 million), and travel expense ($0.4 million). These increases were partially offset by decreases in advertising expense, including trade show fees and related costs ($0.4 million) and bad debt expense ($0.2 million).
Gain on sale-leaseback
Three Months Ended
June 30,
Six Months Ended
June 30,
(In thousands)
2023
2022
2023
2022
Other income, net
2,692
$
—
2,692
$
—
Percentage of sales
19.8
%
—
%
10.5
%
—
%
Durin
g the three and six months ended June 30, 2023, gain on sale-leaseback was approximately $2.7 million as a result of the gain on the sale and leaseback of our Clearwater, FL facility in May 2023.
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APYX MEDICAL CORPORATION
MANAGEMENT'S DISCUSSION AND ANALYSIS OF
FINANCIAL CONDITION AND RESULTS OF OPERATIONS - Continued
Interest Income (Expense)
Three Months Ended
June 30,
Six Months Ended
June 30,
(In thousands)
2023
2022
2023
2022
Interest income
$
179
$
18
$
230
$
20
Percentage of sales
1.3
%
0.2
%
0.9
%
0.1
%
Interest expense
(543)
$
(3)
(777)
$
(11)
Percentage of sales
(4.0)
%
—
%
(3.0)
%
—
%
Interest income increased approximately $0.2 million for both the three and six months ended June 30, 2023, compared with the same periods the prior year. This increase is due to higher yields on our investments in money market funds and U.S. Treasury securities included in cash and cash equivalents, partially offset by a lower average balance.
During the three months ended June 30, 2023, interest expense increased approximately $0.5 million compared with the same period in the prior year. During the six months ended June 30, 2023, interest expense increased approximately $0.7 million. These increases are due to cash and noncash interest expense on the Credit Agreement executed on February 17, 2023.
Income Taxes
Three Months Ended
June 30,
Six Months Ended
June 30,
(In thousands)
2023
2022
Change
2023
2022
Change
Income tax expense (benefit)
$
66
$
96
31.3
%
$
(2,201)
$
166
(1,425.9)
%
Effective tax rate
(6.9)
%
(1.8)
%
32.6
%
(1.5)
%
Our income tax expense was approximately $66,000 and $96,000 with effective tax rates of (6.9)% and (1.8)% for the three months ended June 30, 2023 and 2022, respectively. For the three months ended June 30, 2023 and 2022, the effective rates differ from the statutory rate primarily due to the full valuation allowance recorded on the net operating loss (“NOL”) generated during the period.
Our income tax expense was approximately $(2,201,000) and $166,000 with effective tax rates of 32.6% and (1.5)% for the six months ended June 30, 2023 and 2022, respectively. For the six months ended June 30, 2023, the effective rate differs from the statutory rate primarily due to the reversal of our liability for uncertain tax positions, including accrued interest and penalties of approximately $2.1 million which were sustained upon the completion in January 2023 of the IRS examination of our 2018 through 2020 income tax returns, partially offset by a valuation allowance on the NOL and net deferred tax assets generated during the period. For the six months ended June 30, 2022, the effective rate differs from the statutory rate primarily due to the full valuation allowance recorded on the NOL generated during the period, combined with interest and penalties on uncertain tax positions.
Liquidity and Capital Resources
At June 30, 2023, we had approximately
$18.5 million
in cash and cash equivalents as compared to approximately
$10.2 million
in cash and cash equivalents at December 31, 2022. Our working capital at June 30, 2023 was approximately $33.9 million compared with $31.1 million at December 31, 2022. The increase in working capital at June 30, 2023 was primarily due to the proceeds received upon the sale of our Clearwater, FL facility in May 2023 and the reversal of our liability for uncertain tax positions upon the completion in January 2023 of the IRS examination of our 2018, 2019 and 2020 income tax returns. This increase was partially offset by the net loss incurred by the Company in the first half of 2023, excluding non-cash activity, comprised primarily of stock-based compensation.
For the
six months ended June 30, 2023
, net cash used in operating activities was approximately $6.7 million, which principally funded our loss from operations of $6.8 million, compared with net cash used in operating activities of approximately $10.4 million
in the same period for 2022. As discussed in the Executive Level Overview, our operating loss, cash used in operations and current cash and cash equivalents balance of $18.5 million, of which we must maintain $10.0 million under our Credit
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MANAGEMENT'S DISCUSSION AND ANALYSIS OF
FINANCIAL CONDITION AND RESULTS OF OPERATIONS - Continued
Agreement, raise substantial doubt about our ability to continue as a going concern for a period of at least one year from the date of issuance of our unaudited condensed consolidated financial statements.
In an effort to alleviate these conditions, we pursued various funding solutions in order to improve liquidity.
On November 22, 2022, the we filed a shelf registration statement providing us the ability to register securities in the aggregate amount up to $100 million. The shelf registration included an embedded ATM facility for up to $40 million. To date, we have not utilized this facility.
On February 17, 2023, we entered into a Credit, Security and Guaranty Agreement (the “Credit Agreement”) with MidCap Funding IV Trust (as agent), and MidCap Financial Trust (as term loan servicer), and the lenders party thereto from time to time.
The Credit Agreement provides for an up to $35 million facility, consisting of senior secured term loans and a secured revolving facility. The Credit Agreement provides for senior secured term loans of up to $25 million, comprised of (i) an initial tranche of $10 million, (ii) a second tranche of $5 million, and (iii) a third tranche of $10 million. The secured revolving facility provides for loans in an aggregate principal amount of up to $10 million, subject to a borrowing base equal to certain percentages of the Company’s eligible accounts receivable and inventory, as determined in accordance with the terms of the Credit Agreement.
For a more in depth description of the terms of the Credit Agreement, see Note 7 of Notes to Condensed Consolidated Financial Statements in Item 1 of this report on Form 10-Q.
On February 27, 2023, our Board of Directors approved a plan to sell and leaseback the our real property located in Clearwater, FL. On March 14, 2023, we entered into a Purchase and Sale Agreement (the “Purchase Agreement”) with VK Acquisitions VI, LLC (the “Purchaser”), for the sale of our facility located at 5115 Ulmerton Road, Clearwater, Florida, as more fully described in the Purchase Agreement (collectively, the “Property”) for a purchase price of $7,650,000. On May 8, 2023, we closed on the Purchase Agreement and concurrently executed a 10-year agreement to leaseback the underlying Property from the Purchaser.
For a more in depth description of the terms of the Purchase Agreement, see Notes 4 and 5 of Notes to Condensed Consolidated Financial Statements in Item 1 of this report on Form 10-Q.
During January 2023, we were notified that the IRS examination process of our 2018, 2019 and 2020 tax returns was complete and that the Company's tax refunds were approved for approximately $0.2 million more than the amount recorded in the Company's Consolidated Balance Sheet at December 31, 2022. On August 10, 2023, we received $8.1 million from the IRS, which included approximately $0.4 million of interest on the $7.7 million income tax refunds.
We also continue to re-assess our operating expenditures and cost structure to be commensurate with our expected levels of revenue and we have the ability to reduce or delay expenditures to enhance and preserve liquidity. We have already reduced some operating expenditures, including a reduction-in-force on January 9, 2023, that reduced our U.S. headcount by 14%.
We believe that the actions already taken, and additional actions that we intend to take to manage operating expenditures, will enable us to meet our obligations and our debt covenants for a period of at least one year from the date of issuance of our audited consolidated financial statements. As a result, we believe our plans alleviate substantial doubt about our ability to continue as a going concern. Our audited financial statements do not include any adjustments relating to the carrying amounts and classification of assets and liabilities that may be necessary should we be unable to continue as a going concern.
Net cash provided by investing activities for the six months ended June 30, 2023 was
$7.0 million
related to the sale of our Clearwater, FL facility ($7.3 million), partially offset by investments in property and equipment ($0.3 million). Net cash used in investing activities for the six months ended June 30, 2022 was
$0.7 million related to
investments in property and equipment.
Net cash provided by financing activities for the six months ended June 30, 2023 was
$8.2 million, which primarily related to proceeds received upon the execution of the Credit Agreement ($9.9 million) less debt issuance costs incurred in the transaction ($1.8 million).
At June 30, 2023, our borrowing availability under the revolving facility was approximately $8.0 million.
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MANAGEMENT'S DISCUSSION AND ANALYSIS OF
FINANCIAL CONDITION AND RESULTS OF OPERATIONS - Continued
At June 30, 2023, we had purchase commitments totaling approximately
$3.3 million
, substantially all of which is expected to be purchased within the next twelve months.
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MANAGEMENT'S DISCUSSION AND ANALYSIS OF
FINANCIAL CONDITION AND RESULTS OF OPERATIONS - Continued
Critical Accounting Estimates
In preparing the consolidated financial statements in accordance with accounting principles generally accepted in the United States of America (U.S. GAAP), we have adopted various accounting policies. Our most significant accounting policies are disclosed in Note 2 to the consolidated financial statements included in our 2022
Form 10-K
, filed with the SEC on March 16, 2023.
The preparation of the consolidated financial statements in conformity with U.S. GAAP requires us to make estimates and assumptions that affect the amounts reported in the consolidated financial statements and accompanying notes. Our estimates and assumptions, including those related to inventories, intangible assets, property, plant and equipment, legal proceedings, research and development, warranty obligations, product liability, sales returns and discounts, stock-based compensation and income taxes are updated as appropriate, which in most cases is at least quarterly. We base our estimates on historical experience, or various assumptions that are believed to be reasonable under the circumstances and the results form the basis for making judgments about the reported values of assets, liabilities, revenues and expenses. Actual results may materially differ from these estimates.
Estimates are considered to be critical if they meet both of the following criteria: (1) the estimate requires assumptions about material matters that are uncertain at the time the accounting estimates are made and (2) other materially different estimates could have been reasonably made or material changes in the estimates are reasonably likely to occur from period to period. Our critical accounting estimates include the following:
Stock-based Compensation
Under our stock option plans, options to purchase common shares of the Company may be granted to employees, officers and directors of the Company by the Board of Directors. We account for stock options in accordance with FASB ASC Topic 718-10,
Compensation-Stock Compensation
, with compensation expense recognized over the vesting period. Options are valued using the Black-Scholes model, which includes a number of estimates that affect the amount of our expense. We have determined that the most critical of these estimates are the estimates of expected life and volatility used in the calculations.
Expected life
For employee stock-based compensation awards, we estimate the expected life of awards utilizing the SEC's simplified method. We utilize this method, as we have not historically granted stock-based compensation awards to employees in sufficient volumes to determine a reasonable estimate of the life of awards. For awards granted to non-employees, we calculate expected life using a combination of past exercise behavior, the contractual term and expected remaining exercise behavior.
Volatility
We determine the volatility by utilizing the historical volatility of our stock over the period of the awards expected life. The SEC allows us to include periods in excess of the useful life if we determine that they provide a more reasonable basis for the volatility of our stock. Additionally, ASC 718-10 allows us to exclude periods from the volatility if they pertain to events or circumstances that in our judgment are specific to us and if the event or transaction is not reasonably expected to occur again during the expected term of the awards. We have not included any additional periods, nor disregarded any periods, in calculating our volatility.
Accounts Receivable Allowance
We maintain a reserve for uncollectible accounts receivable. When evaluating the adequacy of the allowance for doubtful accounts, we analyze historical bad debt experience, the composition of outstanding receivables by customer class, and the age of outstanding balances, and we make estimates in connection with establishing the allowance for doubtful accounts, including the expected impacts of changes in the operating environment and other trends. Changes in estimates are reflected in the period they are made. If the financial condition of our customers deteriorates, resulting in an inability to make payments, additional allowances may be required.
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MANAGEMENT'S DISCUSSION AND ANALYSIS OF
FINANCIAL CONDITION AND RESULTS OF OPERATIONS - Continued
Inventory Obsolescence Allowance
We maintain a reserve for excess and obsolete inventory resulting from the potential inability to sell our products at prices in excess of current carrying costs. The markets in which we operate are highly competitive, with new products and surgical procedures introduced on an ongoing basis. Such marketplace changes may cause our products to become obsolete. We make estimates regarding the future recoverability of the costs of these products and record a provision for excess and obsolete inventories based on historical experience and expected future trends. If actual product life cycles, product demand or acceptance of new product introductions are less favorable than projected by management, additional inventory write-downs may be required, which would unfavorably affect future operating results.
Litigation Contingencies
In accordance with authoritative guidance, we record a liability in our consolidated financial statements for these actions when a loss is known or considered probable and the amount can be reasonably estimated. If the reasonable estimate of a known or probable loss is a range, and no amount within the range is a better estimate than any other, the minimum amount of the range is accrued. If a loss is reasonably possible, but not known or probable, and can be reasonably estimated, the estimated loss or range of loss is disclosed in the notes to the consolidated financial statements. In most cases, significant judgment is required to estimate the amount and timing of a loss to be recorded; actual results may differ from these estimates.
Income Taxes
The provision for income taxes includes federal, foreign, state and local income taxes currently payable and those deferred because of temporary differences between the financial statement and tax bases of assets and liabilities. Deferred tax assets or liabilities are computed based on the difference between the financial statement and income tax bases of assets and liabilities using enacted marginal tax rates. Valuation allowances are recorded to reduce deferred tax assets when it is more likely than not that a tax benefit will not be realized. Deferred income tax expenses or credits are based on the changes in the asset or liability from period to period.
As a result of historical losses and our expectation to continue to generate losses in the near future, we recorded a valuation allowance on our net deferred tax assets. Exclusive of the carryback provisions of the CARES Act and the associated income tax benefit recognized in 2020, we do not anticipate recording an income tax benefit related to our deferred tax assets. We will reassess the realization of deferred tax assets each reporting period and will be able to reduce the valuation allowance to the extent our results of operations improve, and it becomes more likely than not that the deferred tax assets will be realized. As Management has not fully determined the timing of when it will generate taxable income in the U.S., we continued to record a valuation allowance on the net deferred tax assets balance as of June 30, 2023.
We assess the financial statement impact of an uncertain tax position taken or expected to be taken on an income tax return at the largest amount that is more-likely-than-not to be sustained upon audit by the relevant taxing authority. An uncertain income tax position will not be recognized in the financial statements unless it is more likely than not of being sustained.
Inflation
The consequences of the pandemic, global supply chain instability and inflationary cost increases and their adverse impact to the global economy, continue to evolve. Accordingly, the significance of the future impact to our business and financial statements remains subject to significant uncertainty. Inflation has not, to date, materially impacted our operations or financial performance. However, as these trends continue for raw materials, freight, and labor costs, our future financial performance could be adversely impacted.
Off-Balance Sheet Arrangements
We have no off-balance sheet arrangements at this time.
Recent Accounting Pronouncements
See Note 2 of
Notes to Condensed Consolidated Financial Statements in Part I, Item 1 of this Form 10-Q
.
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ITEM 3
.
Quantitative and Qualitative Disclosures about Market Risk
Not applicable.
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ITEM 4. Controls and Procedures
Disclosure Controls and Procedures
Our management has established and maintains disclosure controls and procedures that are designed to ensure that the information required to be disclosed by us in reports that we file or submit under the Securities Exchange Act of 1934, as amended (the “Exchange Act”), is recorded, processed, summarized and reported within the time periods specified in the Securities and Exchange Commission's rules and forms, and that such information is accumulated and communicated to management, including the Chief Executive Officer and Chief Financial Officer, as appropriate, to allow timely decisions regarding required disclosure. Management carried out an evaluation, under the supervision and with the participation of our Chief Executive Officer and Chief Financial Officer, of the effectiveness of our disclosure controls and procedures (as such term is defined in Rules 13a-15(e) and 15d-15(e) under the Exchange Act) as of the end of the period covered by this report. Based on such evaluation, our Chief Executive Officer and Chief Financial Officer have concluded that as of June 30, 2023, the Company’s disclosure controls and procedures were effective.
Changes in Internal Control Over Financial Reporting
In February 2023, we entered into a Credit, Security and Guaranty Agreement (“Credit Agreement”). We are in the process of developing new control activities around the accounting for the Credit Agreement, including the review and compliance with debt covenants. There were no other 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 period covered by the Quarterly Report on Form 10-Q that has materially affected, or is reasonably likely to materially affect, our internal control over financial reporting.
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PART II. Other Information
ITEM 1. Legal Proceedings
See Note 1
2
of Notes to Condensed Consolidated Financial Statements in Part I, Item 1 of this Form 10-Q.
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ITEM 1A. Risk Factors
There have been no material changes to the risk factors described under Item 1A of our Annual Report on Form 10-K for the fiscal year ended December 31, 2022.
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ITEM 2. Unregistered Sales of Equity Securities and Use of Proceeds
None.
ITEM 3. Defaults Upon Senior Securities
None.
ITEM 4. Mine Safety Disclosures
Not Applicable.
ITEM 5. Other Information
During the quarter ended June 30, 2023, no director or officer adopted or terminated any contract, instruction or written plan for the purchase or sale of securities of the Company pursuant to Rule 10b5-1(c) or any non-Rule 10b5-1 trading arrangement (as defined in Regulation S-K Item 408), except as set forth below.
On June 26, 2023, Todd Hornsby, our Executive Vice President, temporarily suspended his Rule 10b5-1 trading plan that was originally adopted on March 21, 2023 (the “Hornsby Trading Plan”).
It is anticipated that the suspension of the Hornsby Trading Plan will be rescinded, following the filing and effectiveness of a registration statement with the Commission covering the resale of up to 30,000 shares of the Company’s common stock underlying a certain stock option grant to Mr. Hornsby.
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ITEM 6. Exhibits
3.1
Articles of Incorporation of the Registrant (Incorporated by reference to
Exhibit 3.1 to the Registrant’s report on Form 10-K/A filed on March 31, 2011
)
3.2
By laws of the Registrant (Incorporated by reference to
Exhibit 3.2 to the Registrant’s report on Form 10-K/A filed on March 31, 2011
)
3.3
Certificate of Amendment of the Certificate of Incorporation of the Registrant (Incorporated by reference to
Exhibit 3.5 to the Registrant’s Quarterly Report on Form 10-Q filed on November 3, 2017
)
3.4
Certificate of Elimination (Incorporated by reference to
Exhibit 3.1 to the Registrant’s Current Report on Form 8-K filed on May 3, 2018
)
3.5
Certificate of Amendment of the Certificate of Incorporation of the Registrant (Incorporated by reference to Exhibit 3.1 to the Registrant’s Current Report on Form 8-K filed on December 28, 2018)
10.1
First Amendment to Purchase and Sale Agreement, dated April 12, 2023 (Incorporated by reference to
Exhibit 10.1 to the Registrant’s Current Report on Form 8 filed on April 18, 2023
).
31.1*
Certification pursuant to Section 302 of Sarbanes-Oxley Act of 2002
31.2*
Certification pursuant to Section 302 of Sarbanes-Oxley Act of 2002
32.1*
Certification pursuant to Section 906 of Sarbanes-Oxley Act of 2002
32.2*
Certification pursuant to Section 906 of Sarbanes-Oxley Act of 2002
101.INS**
XBRL Instance Document
101.SCH**
XBRL Taxonomy Extension Schema Document
101.CAL**
XBRL Taxonomy Extension Calculation Linkbase Document
101.DEF**
XBRL Taxonomy Extension Definition Linkbase Document
101.LAB**
XBRL Taxonomy Extension Label Linkbase Document
101.PRE**
XBRL Taxonomy Extension Label Presentation Document
* Filed herewith.
** XBRL (Extensible Business Reporting Language) information is furnished and not filed or a part of registration statement or prospectus for purposes of Sections 11 or 12 of the Securities Act of 1933, as amended is deemed not filed for purposes of Section 18 of the Securities Exchange Act of 1934, as amended and otherwise is not subject to liability under these sections.
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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.
Apyx Medical Corporation
Date: August 10, 2023
By:
/s/ Charles D. Goodwin II
Charles D. Goodwin II
President, Chief Executive Officer and Director
(Principal Executive Officer)
Date: August 10, 2023
By:
/s/ Tara Semb
Tara Semb
Chief Financial Officer,
Treasurer and Secretary
(Principal Financial Officer)
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