0000784199-23-000130.txt : 20230803 0000784199-23-000130.hdr.sgml : 20230803 20230803161107 ACCESSION NUMBER: 0000784199-23-000130 CONFORMED SUBMISSION TYPE: 8-K PUBLIC DOCUMENT COUNT: 14 CONFORMED PERIOD OF REPORT: 20230803 ITEM INFORMATION: Results of Operations and Financial Condition ITEM INFORMATION: Financial Statements and Exhibits FILED AS OF DATE: 20230803 DATE AS OF CHANGE: 20230803 FILER: COMPANY DATA: COMPANY CONFORMED NAME: ARTIVION, INC. CENTRAL INDEX KEY: 0000784199 STANDARD INDUSTRIAL CLASSIFICATION: SURGICAL & MEDICAL INSTRUMENTS & APPARATUS [3841] IRS NUMBER: 592417093 STATE OF INCORPORATION: DE FISCAL YEAR END: 1231 FILING VALUES: FORM TYPE: 8-K SEC ACT: 1934 Act SEC FILE NUMBER: 001-13165 FILM NUMBER: 231140071 BUSINESS ADDRESS: STREET 1: 1655 ROBERTS BOULEVARD N W CITY: KENNESAW STATE: GA ZIP: 30144 BUSINESS PHONE: 7704193355 MAIL ADDRESS: STREET 1: 1655 ROBERTS BOULEVARD N W CITY: KENNESAW STATE: GA ZIP: 30144 FORMER COMPANY: FORMER CONFORMED NAME: CRYOLIFE INC DATE OF NAME CHANGE: 19940526 8-K 1 aort-20230803.htm 8-K aort-20230803
0000784199FALSE00007841992023-08-032023-08-03

UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
WASHINGTON, D.C. 20549
___________________________________________
FORM 8-K
___________________________________________
CURRENT REPORT
PURSUANT TO SECTION 13 OR 15(d) OF THE
SECURITIES EXCHANGE ACT OF 1934
Date of Report (Date of earliest event reported): August 3, 2023
___________________________________________
ARTIVION, INC.
(Exact name of registrant as specified in its charter)
___________________________________________
Delaware1-1316559-2417093
(State or Other Jurisdiction
of Incorporation)
(Commission File Number)
(IRS Employer
Identification No.)
1655 Roberts Boulevard, N.W., Kennesaw, Georgia 30144
(Address of principal executive office) (zip code)
Registrant's telephone number, including area code: (770) 419-3355
___________________________________________________________________________________
(Former name or former address, if changed since last report)
Title of each classTrading Symbol(s)Name of each exchange
on which registered
Common Stock, $0.01 par valueAORTNYSE
___________________________________________
Check the appropriate box below if the Form 8-K filing is intended to simultaneously satisfy the filing obligation of the registrant under any of the following provisions (see General Instruction A.2. below):
Written communications pursuant to Rule 425 under the Securities Act (17 CFR 230.425)
Soliciting material pursuant to Rule 14a-12 under the Exchange Act (17 CFR 240.14a-12)
Pre-commencement communications pursuant to Rule 14d-2(b) under the Exchange Act (17 CFR 240.14d-2(b))
Pre-commencement communications pursuant to Rule 13e-4(c) under the Exchange Act (17 CFR 240.13e-4(c))
Indicate by check mark whether the registrant is an emerging growth company as defined in Rule 405 of the Securities Act of 1933 (§230.405 of this chapter) or Rule 12b-2 of the Securities Exchange Act of 1934 (§240.12b-2 of this chapter).
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.



Item 2.02    Results of Operations and Financial Condition
On August 3, 2023, Artivion, Inc. (“Artivion”) issued a press release announcing its financial results for the second quarter ended June 30, 2023. Artivion hereby incorporates by reference herein the information set forth in its press release dated August 3, 2023, a copy of which is attached hereto as Exhibit 99.1. Except as otherwise provided in the press release, the press release speaks only as of the date of such press release and it shall not create any implication that the affairs of Artivion have continued unchanged since such date.
The information provided pursuant to this Item 2.02 is to be considered “furnished” pursuant to Item 2.02 of Form 8-K and shall not be deemed to be “filed” for purposes of Section 18 of the Securities Exchange Act of 1934, as amended, or otherwise subject to the liabilities of that Section or Sections 11 and 12(a)(2) of the Securities Act of 1933, as amended, nor shall it be deemed incorporated by reference into any of Artivion’s reports or filings with the Securities and Exchange Commission, whether made before or after the date hereof, except as expressly set forth by specific reference in such report or filing.
Except for the historical information contained in this report, the statements made by Artivion are forward-looking statements that involve risks and uncertainties. All such statements are subject to the safe harbor created by the Private Securities Litigation Reform Act of 1995. Artivion’s future financial performance could differ significantly from the expectations of management and from results expressed or implied in the press release.  Please refer to the last paragraph of the text portion of the press release for further discussion about forward-looking statements. For further information on risk factors, please refer to “Risk Factors” contained in Artivion’s most recently filed Form 10-K and its subsequent filings with the Securities and Exchange Commission, as well as in the press release attached as Exhibit 99.1 hereto. Artivion disclaims any obligation or duty to update or modify these forward-looking statements.
Item 9.01(d)    Exhibits
(d)Exhibits.
Exhibit NumberDescription
Press Release dated August 3, 2023.
104Cover Page Interactive Data File (formatted as Inline XBRL and contained in Exhibit 101).
*Furnished herewith, not filed.
-2-


SIGNATURES
Pursuant to the requirements of the Securities Exchange Act of 1934, Artivion, Inc. has duly caused this report to be signed on its behalf by the undersigned hereunto duly authorized.
Date: August 3, 2023
ARTIVION, INC.
By:/s/ D. Ashley Lee
Name:D. Ashley Lee
Title:
Executive Vice President and
Chief Financial Officer
-3-
EX-99.1 2 aort-2023x8k63023ex991.htm EX-99.1 Document
Exhibit 99.1
aort_logoa.jpg
FOR IMMEDIATE RELEASE
Contacts:
ArtivionGilmartin Group LLC
D. Ashley LeeBrian Johnston / Lynn Lewis
Executive Vice President &Phone: 332-895-3222
Chief Financial Officerinvestors@artivion.com
Phone: 770-419-3355
Artivion Reports Second Quarter 2023 Financial Results

Second Quarter and Recent Business Highlights:

Achieved revenue of $89.3 million in the second quarter of 2023 versus $80.3 million in the second quarter of 2022, an increase of 11% on both a GAAP and non-GAAP constant currency basis
Net loss was ($3.4) million or ($0.08) per share; non-GAAP net income was $2.3 million or $0.06 per share
Achieved EBITDA of $9.2 million in the second quarter of 2023; non-GAAP adjusted EBITDA increased 35% to $13.8 million in the second quarter of 2023 compared to the second quarter of 2022
Aortic stent graft revenues increased 19% on both a GAAP and non-GAAP constant currency basis in the second quarter of 2023 compared to the second quarter of 2022
On-X revenues increased 10% on a GAAP basis and 11% on a non-GAAP constant currency basis in the second quarter of 2023 compared to the second quarter of 2022
Received PerClot PMA approval and commenced shipping product to Baxter
Patient enrollment in the PERSEVERE clinical trial accelerated with enrollment completion expected in the third quarter of 2023

ATLANTA, GA – (August 3, 2023) – Artivion, Inc. (NYSE: AORT), a leading cardiac and vascular surgery company focused on aortic disease, today announced its financial results for the second quarter ended June 30, 2023.

“Our second quarter results reflect the strength of our business commercially, operationally, and financially. We delivered double-digit constant currency revenue growth year-over-year for the second consecutive quarter and remain on track to achieve or exceed the revenue and EBITDA growth targets for this year. Our exceptional second quarter performance was driven by year-over-year aortic stent graft revenue growth of 19%, On-X revenue growth of 10%, tissue processing growth of 9%, and BioGlue growth of 4%. On a constant currency basis, year-over-year aortic stent graft, On-X, tissue processing, and BioGlue revenue growth were 19%, 11%, 9%, and 4%, respectively. We also saw Asia Pacific and Latin American revenue grow 23% and 21%, respectively, and 23% and 24% on a constant currency basis, compared to last year,” said Pat Mackin, Chairman, President, and Chief Executive Officer.
Page 1 of 11



Mr. Mackin added, “In addition to our strong commercial results, we also obtained FDA approval for PerClot and, accordingly, received the net $14.3 million FDA approval milestone payment from Baxter. Immediately thereafter, we also began shipping PerClot to Baxter, pursuant to the terms of our agreement. Further, we had strong revenue growth in our aortic stent graft product line, driven by accelerating productivity levels at our German manufacturing facility. We improved patient enrollment for our PERSEVERE trial evaluating AMDS, a simple, elegant stent graft solution to treat aortic arch disease, and we still anticipate completing enrollment in that trial in the third quarter of this year.

Mr. Mackin concluded, “Given our solid execution in the first half of 2023 and strong business momentum, we are now on a path to meet or exceed our current year guidance, as well as to achieve our 2024 commitments to deliver double-digit compounded annual constant currency revenue growth and adjusted EBITDA in excess of $75.0 million.”

Second Quarter 2023 Financial Results
Total revenues for the second quarter of 2023 were $89.3 million, an increase of 11% on both a GAAP and non-GAAP constant currency basis, both compared to the second quarter of 2022.

Net loss for the second quarter of 2023 was ($3.4) million, or ($0.08) per fully diluted common share, compared to net loss of ($4.3) million, or ($0.11) per fully diluted common share for the second quarter of 2022. Net loss for the second quarter of 2023 includes pretax charges of $10.9 million related to contingent consideration for the acquisition of AMDS and $5.0 million related to the final payment to Endospan under our September 2019 Loan Agreement with Endospan, partially offset by a net pretax gain of $14.3 million related to the PerClot PMA approval milestone net payment. Non-GAAP net income for the second quarter of 2023 was $2.3 million, or $0.06 per fully diluted common share, compared to non-GAAP net loss of ($1.3) million, or ($0.03) per fully diluted common share for the second quarter of 2022.

2023 Financial Outlook
Artivion is raising its revenue guidance range and now expects to achieve constant currency revenue growth of between 10% and 12%, compared to the previous range of 9% and 12%, for the full year 2023 compared to 2022. The Company expects revenues to be in a range of $342.0 million and $350.0 million, compared to the previous range of $337.0 million and $348.0 million.

Additionally, Artivion continues to expect adjusted EBITDA, as reported, to increase greater than 25% in 2023 compared to 2022, resulting in adjusted EBITDA in excess of $52.0 million for 2023.

The Company's financial performance for 2023 and future periods is subject to the risks identified below.

Page 2 of 11


Non-GAAP Financial Measures
This press release contains non-GAAP financial measures, including non-GAAP revenue, non-GAAP net income, non-GAAP EBITDA, and non-GAAP general, administrative, and marketing expenses. Investors should consider this non-GAAP information in addition to, and not as a substitute for, financial measures prepared in accordance with US GAAP. In addition, this non-GAAP financial information may not be the same as similar measures presented by other companies. The Company's non-GAAP revenues are adjusted for the impact of changes in currency exchange. The Company’s non-GAAP net income; non-GAAP EBITDA; and non-GAAP general, administrative, and marketing results exclude (as applicable) depreciation and amortization expense; interest income and expense; stock-based compensation expense; loss or gain on foreign currency revaluation; income tax expense or benefit; corporate rebranding expense; business development, integration, and severance income or expense; non-cash interest expense; gain from sale of non-financial assets, and abandonment of CardioGenesis cardiac laser therapy business. The Company generally uses non-GAAP financial measures to facilitate management's review of the operational performance of the company and as a basis for strategic planning. Company management believes that these non-GAAP presentations provide useful information to investors regarding unusual non-operating transactions; the operating expense structure of the Company's existing and recently acquired operations, without regard to its on-going efforts to acquire additional complementary products and businesses, and the transaction and integration expenses incurred in connection with recently acquired and divested product lines; and the operating expense structure excluding fluctuations resulting from foreign currency revaluation and stock-based compensation expense. The Company believes it is useful to exclude certain expenses because such amounts in any specific period may not directly correlate to the underlying performance of its business operations or can vary significantly between periods as a result of factors such as impact of recent acquisitions, non-cash expense related to amortization of previously acquired tangible and intangible assets, and any related adjustments to their carrying values. The Company has adjusted for the impact of changes in currency exchange from certain revenues to evaluate comparable product growth rates on a constant currency basis. The Company does, however, expect to incur similar types of expenses and currency exchange impacts in the future, and this non-GAAP financial information should not be viewed as a statement or indication that these types of expenses will not recur. Company management encourages investors to review the Company's consolidated financial statements and publicly filed reports in their entirety, including the reconciliation of GAAP to non-GAAP financial measures.”

Webcast and Conference Call Information
The Company will hold a teleconference call and live webcast later today, August 3, 2023, at 4:30 p.m. ET to discuss the results, followed by a question and answer session. To participate in the conference call dial 201-689-8261 a few minutes prior to 4:30 p.m. ET. The teleconference replay will be available approximately one hour following the completion of the event and can be accessed by calling (toll free) 877-660-6853 or 201-612-7415. The conference number for the replay is 13739398.

The live webcast and replay can be accessed by going to the Investors section of the Artivion website at www.Artivion.com and selecting the heading Webcasts & Presentations.

Page 3 of 11


About Artivion, Inc.
Headquartered in suburban Atlanta, Georgia, Artivion, Inc. is a medical device company focused on developing simple, elegant solutions that address cardiac and vascular surgeons’ most difficult challenges in treating patients with aortic diseases. Artivion’s four major groups of products include: aortic stent grafts, surgical sealants, On-X mechanical heart valves, and implantable cardiac and vascular human tissues. Artivion markets and sells products in more than 100 countries worldwide. For additional information about Artivion, visit our website, www.artivion.com.

Forward Looking Statements
Statements made in this press release that look forward in time or that express management's beliefs, expectations, or hopes are forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. Such forward-looking statements reflect the views of management at the time such statements are made. These statements include our beliefs that we remain on track to achieve or exceed the revenue and EBITDA growth targets for this year; and we are now on a path to meet or exceed our current year guidance, as well as to achieve our 2024 commitments to deliver double-digit compounded annual constant currency revenue growth and adjusted EBITDA in excess of $75.0 million. These forward-looking statements are subject to a number of risks, uncertainties, estimates, and assumptions that may cause actual results to differ materially from current expectations, including that the benefits anticipated from the Ascyrus Medical LLC transaction and Endospan agreements may not be achieved at all or at the levels we had originally anticipated; the benefits anticipated from our clinical trials may not be achieved or achieved on our anticipated timeline; our products may not be able to consistently retain their existing regulatory approvals or special regulatory approvals in order to be commercialized; products in our pipeline may not receive regulatory approval at all or receive regulatory approval on our anticipated timelines; or our products that obtain regulatory approval may not be adopted by the market as much as we anticipate or at all. These risks and uncertainties include the risk factors detailed in our Securities and Exchange Commission filings, including our Form 10-K for the year ended December 31, 2022 and our Form 10-Q for the quarter ended June 31, 2023. Artivion does not undertake to update its forward-looking statements, whether as a result of new information, future events, or otherwise.
Page 4 of 11


Artivion, Inc. and Subsidiaries
Condensed Consolidated Statements of Operations and Comprehensive Loss
In Thousands, Except Per Share Data
(Unaudited)

Three Months Ended
June 30,
Six Months Ended
June 30,
2023202220232022
Revenues:
Products$66,003 $58,936 $128,294 $116,478 
Preservation services23,248 21,404 44,186 41,075 
Total revenues89,251 80,340 172,480 157,553 
Cost of products and preservation services:
Products20,977 18,230 40,510 35,638 
Preservation services10,190 9,938 20,159 19,024 
Total cost of products and preservation services31,167 28,168 60,669 54,662 
Gross margin58,084 52,172 111,811 102,891 
Operating expenses:
General, administrative, and marketing57,241 38,983 107,606 77,938 
Research and development7,418 8,648 14,641 18,776 
Total operating expenses64,659 47,631 122,247 96,714 
Gain from sale of non-financial assets(14,250)— (14,250)— 
Operating income7,675 4,541 3,814 6,177 
Interest expense6,356 4,101 12,452 8,049 
Interest income(265)(30)(340)(46)
Other expense, net4,241 3,770 3,278 3,903 
Loss before income taxes(2,657)(3,300)(11,576)(5,729)
Income tax expense725 959 5,338 1,919 
Net loss$(3,382)$(4,259)$(16,914)$(7,648)
Loss per share:
Basic$(0.08)$(0.11)$(0.41)$(0.19)
Diluted$(0.08)$(0.11)$(0.41)$(0.19)
Weighted-average common shares outstanding:
Basic 40,755 40,031 40,595 39,941 
Diluted40,755 40,031 40,595 39,941 
Net loss$(3,382)$(4,259)$(16,914)$(7,648)
Other comprehensive loss:
Foreign currency translation adjustments1,826 (14,796)5,442 (18,571)
Comprehensive loss$(1,556)$(19,055)$(11,472)$(26,219)
Page 5 of 11


Artivion, Inc. and Subsidiaries
Condensed Consolidated Balance Sheets
In Thousands
June 30,
2023
December 31,
2022
(Unaudited)
ASSETS
Current assets:
Cash and cash equivalents$48,775 $39,351 
Trade receivables, net64,806 61,820 
Other receivables4,450 7,764 
Inventories, net78,458 74,478 
Deferred preservation costs, net48,302 46,371 
Prepaid expenses and other19,107 17,550 
Total current assets263,898 247,334 
Goodwill245,561 243,631 
Acquired technology, net147,029 151,263 
Operating lease right-of-use assets, net40,825 41,859 
Property and equipment, net38,389 38,674 
Other intangibles, net29,966 31,384 
Deferred income taxes3,951 1,314 
Other assets8,242 7,339 
Total assets$777,861 $762,798 
LIABILITIES AND SHAREHOLDERS' EQUITY
Current liabilities:
Accounts payable$10,455 $12,004 
Accrued expenses10,365 12,374 
Accrued compensation12,792 13,810 
Taxes payable10,641 2,635 
Current maturities of operating leases4,037 3,308 
Accrued procurement fees1,744 2,111 
Current portion of long-term debt1,561 1,608 
Other liabilities4,635 1,825 
Total current liabilities56,230 49,675 
Long-term debt306,109 306,499 
Contingent consideration 56,100 40,400 
Non-current maturities of operating leases39,989 41,257 
Deferred income taxes19,469 24,499 
Deferred compensation liability6,541 5,468 
Non-current finance lease obligation3,446 3,644 
Other liabilities7,469 7,027 
Total liabilities$495,353 $478,469 
Commitments and contingencies
Shareholders' equity:
Preferred stock— — 
Common stock (75,000 shares authorized, 42,443 and 41,830 shares issued and outstanding in 2023 and 2022, respectively)424 418 
Additional paid-in capital347,030 337,385 
Retained deficit (34,131)(17,217)
Accumulated other comprehensive loss (16,167)(21,609)
Treasury stock, at cost, 1,487 shares as of June 30, 2023 and December 31, 2022(14,648)(14,648)
Total shareholders' equity282,508 284,329 
Total liabilities and shareholders' equity$777,861 $762,798 
Page 6 of 11


Artivion, Inc. and Subsidiaries
Condensed Consolidated Statement of Cash Flows
In Thousands
(Unaudited)
Six Months Ended
June 30,
20232022
Net cash flows from operating activities:
Net loss$(16,914)$(7,648)
Adjustments to reconcile net loss to net cash from operating activities:
Change in fair value of contingent consideration15,700 (5,000)
Depreciation and amortization11,501 11,497 
Non-cash compensation7,279 6,100 
Fair value adjustment of long-term loan 5,000 — 
Non-cash lease expense 3,631 3,803 
Write-down of inventories and deferred preservation costs2,021 2,177 
Deferred income taxes(8,073)(1,611)
Gain from sale of non-financial assets(14,250)— 
Other 1,836 940 
Changes in operating assets and liabilities:
Accounts payable, accrued expenses, and other liabilities1,607 (5,677)
Receivables655 (9,635)
Prepaid expenses and other assets(2,317)(205)
Inventories and deferred preservation costs(6,921)(3,653)
Net cash flows provided by (used in) operating activities755 (8,912)
Net cash flows from investing activities:
Proceeds from sale of non-financial assets, net14,250 — 
Capital expenditures(4,029)(4,055)
Payments for Endospan Agreement(5,000)— 
Other(986)(939)
Net cash flows provided by (used in) investing activities4,235 (4,994)
Net cash flows from financing activities:
Proceeds from financing insurance premiums3,558 — 
Proceeds from exercise of stock options and issuance of common stock2,581 2,318 
Principal payments on short-term notes payable(529)— 
Redemption and repurchase of stock to cover tax withholdings(563)(1,739)
Repayment of term loan(1,381)(1,370)
Other(262)(241)
Net cash flows provided by (used in) financing activities3,404 (1,032)
Effect of exchange rate changes on cash and cash equivalents1,030 310 
Increase (decrease) in cash and cash equivalents9,424 (14,628)
Cash and cash equivalents beginning of period39,351 55,010 
Cash and cash equivalents end of period$48,775 $40,382 
Page 7 of 11


Artivion, Inc. and Subsidiaries
Financial Highlights
In Thousands
(Unaudited)
Three Months Ended
June 30,
Six Months Ended
June 30,
2023202220232022
Products:
Aortic stent grafts$28,359$23,833$54,509$49,339
On-X17,94616,25535,60230,626
Surgical sealants16,56615,96733,26931,648
Other3,1322,8814,9144,865
Total products66,00358,936128,294 116,478 
Preservation services 23,24821,40444,18641,075
Total revenues$89,251$80,340$172,480$157,553
Revenues:
US$44,425$40,953$85,758$78,688
    International44,82639,387$86,72278,865
Total revenues$89,251$80,340$172,480 $157,553 
Page 8 of 11


Artivion, Inc. and Subsidiaries
Reconciliation of GAAP to Non-GAAP
Revenues and General, Administrative, and Marketing Expense
In Thousands
(Unaudited)
Revenues for the
Three Months Ended
June 30,
Percent
Change
From Prior
Year
20232022
US GAAPUS GAAPExchange rate effectConstant CurrencyConstant Currency
Products:
Aortic stent grafts$28,359$23,83329 $23,86219%
On-X17,94616,255(72)16,18311%
Surgical sealants16,56615,967(69)15,8984%
Other3,1322,881(4)2,8779%
Total products66,00358,936(116)58,82012%
Preservation services23,24821,404(34)21,3709%
Total$89,251$80,340$(150)$80,19011%
Revenues for the
Six Months Ended
June 30,
Percent
Change
From Prior
Year
20232022
US GAAPUS GAAPExchange rate effectConstant CurrencyConstant Currency
Products:
Aortic stent grafts$54,509$49,339(1,209)$48,13013%
On-X35,60230,626(219)30,40717%
Surgical sealants33,26931,648(354)31,2946%
Other4,9144,865(19)4,8461%
Total products128,294116,478(1,801)114,67712%
Preservation services44,18641,075(69)41,0068%
Total$172,480$157,553$(1,870)$155,68311%
Three Months Ended
June 30,
Six Months Ended
June 30,
2023202220232022
Reconciliation of G&A expense, GAAP to adjusted G&A, non-GAAP:
General, administrative, and marketing expense, GAAP$57,241 $38,983 $107,606 $77,938 
  Business development, integration, and severance expense (income)11,101 (3,101)16,098 (4,680)
  Corporate rebranding expense69 289 218 1,172 
  Abandonment of CardioGenesis cardiac laser therapy business 160 — 160 — 
Adjusted G&A, non-GAAP$45,911 $41,795 $91,130 $81,446 
Page 9 of 11


Artivion, Inc. and Subsidiaries
Reconciliation of GAAP to Non-GAAP
Adjusted EBITDA
In Thousands
(Unaudited)

Three Months Ended
June 30,
Six Months Ended
June 30,
2023202220232022
Reconciliation of net loss, GAAP to adjusted EBITDA, non-GAAP:
Net loss, GAAP$(3,382)$(4,259)$(16,914)$(7,648)
Adjustments:
  Business development, integration, and severance expense (income)15,270 (3,101)20,722 (4,680)
Interest expense6,356 4,101 12,452 8,049 
Depreciation and amortization expense5,767 5,616 11,501 11,497 
Stock-based compensation expense3,938 2,934 7,279 6,100 
Income tax expense725 959 5,338 1,919 
Abandonment of CardioGenesis cardiac laser therapy business390 — 390 — 
Corporate rebranding expense69 289 218 1,172 
Interest income(265)(30)(340)(46)
(Gain) loss on foreign currency revaluation(797)3,754 (1,770)3,887 
Gain from sale of non-financial assets(14,250)— (14,250)— 
Adjusted EBITDA, non-GAAP$13,821 $10,263 $24,626 $20,250 
Page 10 of 11


Artivion Inc. and Subsidiaries
Reconciliation of GAAP to Non-GAAP
Net Income and Diluted Income Per Common Share
In Thousands, Except Per Share Data
(Unaudited)
Three Months Ended
June 30,
Six Months Ended
June 30,
2023202220232022
GAAP:
Loss before income taxes$(2,657)$(3,300)$(11,576)$(5,729)
Income tax expense725 959 5,338 1,919 
Net loss$(3,382)$(4,259)$(16,914)$(7,648)
Diluted loss per common share$(0.08)$(0.11)$(0.41)$(0.19)
Diluted weighted-average common shares outstanding40,755 40,031 40,595 39,941 
Reconciliation of loss before income taxes, GAAP to adjusted income (loss), non-GAAP:
Loss before income taxes, GAAP:$(2,657)$(3,300)$(11,576)$(5,729)
Adjustments:
Business development, integration, and severance expense (income)15,270 (3,101)20,722 (4,680)
Amortization expense3,806 3,905 7,687 7,989 
Non-cash interest expense464 457 926 913 
Abandonment of CardioGenesis cardiac laser therapy business390 — 390 — 
Corporate rebranding expense69 289 218 1,172 
Gain from sale of non-financial assets(14,250)— (14,250)— 
Adjusted income (loss) before income taxes, non-GAAP3,092 (1,750)4,117 (335)
Income tax expense (benefit) calculated at a tax rate of 25%773 (438)1,029 (84)
Adjusted net income (loss), non-GAAP$2,319 $(1,312)$3,088 $(251)
Reconciliation of diluted loss per common share, GAAP to adjusted diluted income (loss) per common share, non-GAAP:
Diluted loss per common share, GAAP:$(0.08)$(0.11)$(0.41)$(0.19)
Adjustments:
Business development, integration, and severance expense (income)0.37 (0.08)0.50 (0.12)
Effect of 25% tax rate0.03 0.05 0.20 0.08 
Amortization expense0.09 0.10 0.19 0.20 
Non-cash interest expense0.01 0.01 0.02 0.02 
Abandonment of CardioGenesis cardiac laser therapy business0.01 — 0.01 — 
Corporate rebranding expense— 0.01 0.01 0.03 
Tax effect of non-GAAP adjustments(0.03)(0.01)(0.10)(0.03)
Gain from sale of non-financial assets(0.34)— (0.34)— 
Adjusted diluted income (loss) per common share, non-GAAP$0.06 $(0.03)$0.08 $(0.01)
Reconciliation of diluted weighted-average common shares outstanding GAAP to diluted weighted-average common shares outstanding, non-GAAP:
Diluted weighted-average common shares outstanding, GAAP:40,755 40,031 40,595 39,941 
Adjustments:
Effect of dilutive stock options and awards419 — 444 — 
Diluted weighted-average common shares outstanding, non-GAAP41,174 40,031 41,039 39,941 
Page 11 of 11
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Cover
Aug. 03, 2023
Cover [Abstract]  
Document Type 8-K
Document Period End Date Aug. 03, 2023
Entity Registrant Name ARTIVION, INC.
Entity Incorporation, State or Country Code DE
Entity File Number 1-13165
Entity Tax Identification Number 59-2417093
Entity Address, Address Line One 1655 Roberts Boulevard, N.W.,
Entity Address, City or Town Kennesaw
Entity Address, State or Province GA
Entity Address, Postal Zip Code 30144
City Area Code 770
Local Phone Number 419-3355
Title of 12(b) Security Common Stock, $0.01 par value
Trading Symbol AORT
Security Exchange Name NYSE
Written Communications false
Soliciting Material false
Pre-commencement Tender Offer false
Pre-commencement Issuer Tender Offer false
Entity Emerging Growth Company false
Entity Central Index Key 0000784199
Amendment Flag false
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