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AORT Positive Sentiment Score: 75/100

Artivion Gilmartin Group LLC Lance A. Berry Brian Johnston Laine Morgan Executive Vice President Phone 332-895-3222 Chief Financial Officer investors artivion.com Phone 770-419-3355 Artivio

Key Takeaway: Artivion reported its financial results for the fourth quarter and full year 2024, noting a revenue increase of 4% in Q4 and 10% for the entire year. The company achieved adjusted EBITDA growth of 15% in Q4 and 32% for the full year, highlighting operational strength despite a net loss of $16.5 million in Q4. Key achievements included receiving a Humanitarian Device Exemption for the AMDS Hybrid Prosthesis and submitting the second module of the PMA application to the FDA. Looking ahead, Artivion projects revenue growth of 10% to 14% for 2025 while acknowledging potential impacts from foreign currency fluctuations.

Market Sentiment Analysis

POSITIVE FACTORS

  • Fourth quarter revenue increased by 4% year-over-year.
  • Adjusted EBITDA rose by 15% in the fourth quarter, indicating strong operational performance.
  • Humanitarian Device Exemption granted by the FDA for AMDS Hybrid Prosthesis enhances commercial potential.

CONCERNS & RISKS

  • Net loss increased to $16.5 million in Q4, higher than the previous year's loss.
  • Foreign currency revaluation impacted non-GAAP net income in Q4.

Full Press Release Details

Artivion Gilmartin Group LLC
Lance A. Berry Brian Johnston Laine Morgan
Executive Vice President Phone 332-895-3222
Chief Financial Officer investors artivion.com
Phone 770-419-3355
Artivion Reports Fourth Quarter and Full Year 2024 Financial Results
Fourth Quarter Highlights
Achieved revenue of $97.3 million in the fourth quarter of 2024 versus $93.7 million in the fourth quarter of 2023, an increase of 4% on a GAAP basis and 3% on a non-GAAP constant currency basis
Achieved revenue of $388.5 million for the full year of 2024 versus $354.0 million for the full year of 2023, an increase of 10% on a GAAP basis and 9% on a non-GAAP constant currency basis
Net loss was $(16.5) million, or $(0.39) per fully diluted share and non-GAAP net income was $0.2 million, or $0.00 per fully diluted share in the fourth quarter of 2024. For the full year, net loss was $(13.4) million, compared to a net loss of $(30.7) million in the 2023 fiscal year
Adjusted EBITDA increased 15% to $17.6 million in the fourth quarter of 2024 compared to $15.3 million in the fourth quarter of 2023. For the full year adjusted EBITDA increased 32% to $71.3 million
Generated $22.2 million of operating cash flow and $11.0 million of non-GAAP free cash flow for the full year of 2024
Granted Humanitarian Device Exemption (HDE) by the U.S. Food and Drug Administration (FDA) for the AMDS Hybrid Prosthesis
Submitted second module of the pre-market approval application (PMA) to the FDA for AMDS Hybrid Prosthesis
ATLANTA, GA - (February 24, 2025) - Artivion, Inc. (NYSE AORT), a leading cardiac and vascular surgery company focused on aortic disease, today announced financial results for the fourth quarter and year ended December 31, 2024.
"2024 was an excellent year for Artivion, marked by robust revenue and adjusted EBITDA growth, which enabled us to deliver positive free cash flow while making significant strides in key clinical and regulatory initiatives. Revenue growth in the fourth quarter was driven by year-over-year growth in On-X of 10%, stent grafts of 10%, and BioGlue of 8% all compared to the fourth quarter of 2023. On a constant currency basis, year-over-year, On-X, stent grafts, and BioGlue grew 10%, 8%, and 7%, respectively. We also saw continued revenue strength in Latin America which grew 26% both in the fourth quarter and for the full year 2024 on a constant currency basis compared to last year." said Pat Mackin, Chairman, President, and Chief Executive Officer.
Mr. Mackin continued, "In addition to our commercial results, we were also thrilled to receive a Humanitarian Device Exemption from the FDA for AMDS. This enables us to deliver our groundbreaking, life-saving technology to patients while we continue to work with the FDA toward PMA approval."
Mr. Mackin added, "Q4 was a continuation of the outstanding progress we saw this year on multiple clinical and regulatory fronts. First, new clinical data from our AMDS PERSEVERE trial was presented in a Late-Breaking Science session at the Society of Thoracic Surgeons. It demonstrated sustained benefit of AMDS out to one-year, including a 50% reduction in mortality at one-year as compared to the reference cohort. Second, we submitted our second module of the PMA application to the FDA for AMDS."
Mr. Mackin concluded, "Finally, I'd like to thank our team members for their dedication to mitigating the late November 2024 cybersecurity incident and maintaining our ability to continue serving our customers and their patients. Thanks to their hard work, we are operating at normal levels across the business, with any remaining inefficiencies expected to be resolved in the near-term. While our Q4 revenues were negatively impacted, we do not expect this incident to meaningfully impact our business for the full year 2025. Looking ahead for 2025, we remain confident in our ability to execute on our best-in-class pipeline and drive sustained double-digit revenue growth and adjusted EBITDA growth at twice the pace of constant currency revenue growth.
Fourth Quarter 2024 Financial Results
Total revenues for the fourth quarter of 2024 were $97.3 million, an increase of 4% on a GAAP basis and 3% on a non-GAAP constant currency basis, both compared to the fourth quarter of 2023.
Net loss for the fourth quarter of 2024 was $(16.5) million, or $(0.39) per fully diluted common share, compared to net loss of $(4.0) million, or $(0.10) per fully diluted common share for the fourth quarter of 2023. Non-GAAP net income for the fourth quarter of 2024 was $0.2 million, or $0.00 per fully diluted common share, compared to non-GAAP net income of $4.6 million, or $0.11 per fully diluted common share for the fourth quarter of 2023. Non-GAAP net income for the fourth quarter of 2024 includes pretax losses related to foreign currency revaluation of $5.4 million.
Full Year 2024 Financial Results
Total revenues for 2024 were $388.5 million, an increase of 10% on a GAAP basis and 9% on a non-GAAP constant currency basis, both compared to the full year of 2023.
Net loss for 2024 was $(13.4) million, or $(0.32) per fully diluted common share, compared to net loss of $(30.7) million, or $(0.75) per fully diluted common share for the full year of 2023. Non-GAAP net income for the full year of 2024 was $10.8 million, or $0.25 per fully diluted common share, compared to non-GAAP net income of $8.4 million, or $0.20 per fully diluted common share for the full year of 2023. Non-GAAP net income for the full year of 2024 includes pretax losses related to foreign currency revaluation of $5.4 million.
2025 Financial Outlook
Artivion expects revenues for the full year 2025 to be in the range of $420 to $435 million, representing growth of 10% to 14% on a constant currency basis compared to 2024. At current exchange rates, the Company expects currency to negatively impact year-over-year as reported revenue growth rates by approximately 2%.
Additionally, Artivion expects adjusted EBITDA growth of between 18% and 28% for the full year 2025 compared to 2024, resulting in an expected range of $84 to $91 million for 2025.
The Company's financial performance for 2025 and future periods is subject to the risks identified below.
Non-GAAP Financial Measures
This press release contains non-GAAP financial measures, including non-GAAP revenue, non-GAAP net income, EBITDA, adjusted EBITDA, non-GAAP general, administrative, and marketing expenses, and free cash flows. 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, EBITDA, adjusted EBITDA, general, administrative, and marketing, and free cash flows results primarily exclude (as applicable) depreciation and amortization expense, interest income and expense, non-cash compensation expense, loss or gain on foreign currency revaluation, income tax expense or benefit, business development, integration, and severance income or expense, loss on extinguishment of debt, non-cash interest expense, capital expenditures, and other non-recurring items.
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 non-cash compensation expense. The Company believes it is useful to exclude certain expenses and revenues 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.
The Company's adjusted EBITDA expectations for fiscal 2025 exclude potential charges or gains that may be recorded during the fiscal year, relating to, among other things, non-cash compensation business development, integration, and severance income or expense loss on extinguishment of debt and foreign currency revaluations. The Company does not attempt to provide reconciliations of forward-looking adjusted EBITDA to the comparable GAAP measure because the impact and timing of these potential charges or gains are inherently uncertain and difficult to predict and are unavailable without unreasonable efforts. In addition, the Company believes such reconciliations would imply a degree of precision and certainty that could be confusing to investors. Such items could have a material impact on GAAP measures of the Company's financial performance.
Webcast and Conference Call Information
The Company will hold a teleconference call and live webcast on February 24, 2025, 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 13749878.
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.
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, but are not limited to, our beliefs and expectations about our revenue, year-over-year growth and growth drivers, earnings, currency impacts, and other financial measures and related information our anticipated capital needs and capital structure our beliefs about our competitive advantages and market opportunities our expected product mix anticipated quarterly fluctuations in our business the timeline for regulatory approval for AMDS and other products the benefits of receiving the Humanitarian Device Exemption and Breakthrough Designation for AMDS our expected geographies and timeframes for commercializing our products that our revenues for the full year 2025 will be in the range of $420 to $435 million, representing revenue growth of between 10% to 14% compared to 2024 on a constant currency basis that we expect, at current exchange rates, a negative 2% currency impact on the 2025 full year revenues our beliefs and expectations about the impact of the November 2024 cybersecurity incident and that we expect non-GAAP adjusted EBITDA to increase between 18% and 28% for the full year 2025 compared to 2024, resulting in non-GAAP adjusted EBITDA in the range of $84 to $91 million in 2025. 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, but not limited to, the unpredictability of the timing and outcome of regulatory decisions and other regulatory developments risks relating to our international operations the benefits anticipated from our new credit facility, the Ascyrus Medical LLC transaction and Endospan agreements, and our operational improvements in our tissue and stent graft business may not be achieved at all or at the levels we anticipate or had originally anticipated the benefits anticipated from our clinical trials and regulatory approvals may not be achieved or achieved on our anticipated timelines the uncertainty regarding potential unknown or future impacts of the November 2024 cybersecurity incident and the benefits anticipated from our expansion into APAC and LATAM may not be achieved or achieved on our anticipated timelines. 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, 2024. Artivion does not undertake to update its forward-looking statements, whether as a result of new information, future events, or otherwise.
Artivion, Inc. and Subsidiaries
Consolidated Statements of Operations and Comprehensive Loss
In Thousands, Except Per Share Data
Three Months Ended December 31, Year Ended December 31,
2024 2023 2024 2023
(Unaudited) (Unaudited)
Revenues
Products $ 74,662 $ 69,144 $ 290,230 $ 261,185
Preservation services 22,646 24,526 98,307 92,819
Total revenues 97,308 93,670 388,537 354,004
Cost of products and preservation services
Products 26,678 22,511 99,385 84,595
Preservation services 9,128 10,064 40,371 40,233
Total cost of products and preservation services 35,806 32,575 139,756 124,828
Gross margin 61,502 61,095 248,781 229,176
Operating expenses
General, administrative, and marketing 51,429 50,278 181,455 208,977
Research and development 7,404 7,645 28,452 28,707
Total operating expenses 58,833 57,923 209,907 237,684
Gain from sale of non-financial assets - - - (14,250)
Operating income 2,669 3,172 38,874 5,742
Interest expense 9,742 6,244 34,277 25,299
Interest income (374) (398) (1,467) (1,077)
Loss on extinguishment of debt - - 3,669 -
Other expense (income), net 9,903 (2,083) 9,909 3,106
Loss before income taxes (16,602) (591) (7,514) (21,586)
Income tax (benefit) expense (119) 3,384 5,845 9,104
Net loss $ (16,483) $ (3,975) $ (13,359) $ (30,690)
Loss per share
Basic $ (0.39) (0.10) $ (0.32) $ (0.75)
Diluted $ (0.39) $ (0.10) $ (0.32) $ (0.75)
Weighted-average common shares outstanding
Basic 41,882 40,898 41,676 40,743
Diluted 41,882 40,898 41,676 40,743
Net loss $ (16,483) $ (3,975) $ (13,359) $ (30,690)
Other comprehensive (loss) income
Foreign currency translation adjustments (15,399) 9,167 (12,917) 9,599
Comprehensive (loss) income $ (31,882) $ 5,192 $ (26,276) $ (21,091)
Artivion, Inc. and Subsidiaries
Consolidated Balance Sheets
December 31,
2024 2023
(Unaudited)
ASSETS
Current assets
Cash and cash equivalents $ 53,463 $ 58,940
Trade receivables, net 79,462 71,796
Other receivables 6,431 2,342
Inventories 79,766 81,976
Deferred preservation costs 51,701 49,804
Prepaid expenses and other 19,257 15,810
Total current assets 290,080 280,668
Goodwill 240,958 247,337
Acquired technology, net 128,051 142,593
Operating lease right-of-use assets, net 39,726 43,822
Property and equipment, net 36,403 38,358
Other intangibles, net 28,332 29,638
Deferred tax assets, net 1,068 1,087
Other long-term assets 24,483 8,894
Total assets $ 789,101 $ 792,397
Artivion, Inc. and Subsidiaries
Consolidated Balance Sheets
In Thousands, Except Par Value
December 31,
2024 2023
(Unaudited)
LIABILITIES AND STOCKHOLDERS' EQUITY
Current liabilities
Accounts payable $ 17,971 $ 13,318
Accrued compensation 18,342 18,715
Accrued expenses 11,834 10,449
Accrued interest 8,170 2,283
Taxes payable 2,934 3,840
Accrued procurement fees 1,704 1,439
Current maturities of operating leases 4,489 3,395
Current portion of finance lease obligations 601 582
Current portion of long-term debt, net 195 1,451
Other current liabilities 583 2,390
Total current liabilities 66,823 57,862
Long-term debt, net 314,152 305,531
Contingent consideration 52,880 63,890
Non-current maturities of operating leases 39,988 43,977
Deferred tax liabilities, net 20,183 21,851
Deferred compensation liability 7,977 6,760
Non-current finance lease obligations 2,833 3,405
Other long-term liabilities 8,065 7,341
Total liabilities 512,901 510,617
Commitments and contingencies
Stockholders' equity
Preferred stock $0.01 par value per share, 5,000 shares authorized, no shares issued - -
Common stock $0.01 par value per share, 75,000 shares authorized, 43,432 and 42,569 shares issued as of December 31, 2024 and 2023, respectively 434 426
Additional paid-in capital 376,607 355,919
Retained deficit (61,266) (47,907)
Accumulated other comprehensive loss (24,927) (12,010)
Treasury stock at cost, 1,487 shares as of December 31, 2024 and 2023 (14,648) (14,648)
Total stockholders' equity 276,200 281,780
Total liabilities and stockholders' equity $ 789,101 $ 792,397
Artivion, Inc. and Subsidiaries
Consolidated Statement of Cash Flows
Year Ended December 31,
2024 2023
(Unaudited)
Net cash flows from operating activities
Net loss $ (13,359) $ (30,690)
Adjustments to reconcile net loss to net cash from operating activities
Depreciation and amortization 24,205 23,076
Non-cash compensation 14,242 14,422
Non-cash lease expense 4,915 4,541
Write-down of inventories and deferred preservation costs 4,434 4,785
Non-cash interest expense 3,866 1,858
Deferred income taxes (1,511) (1,385)
Change in fair value of contingent consideration (11,010) 23,490
Endospan fair value adjustments 4,329 5,000
Loss on extinguishment of debt 3,669 -
Gain on sale of non-financial assets - (14,250)
Other 5,699 1,358
Changes in operating assets and liabilities
Receivables (15,395) (4,050)
Inventories and deferred preservation costs (6,137) (14,360)
Prepaid expenses and other assets (5,209) 535
Accounts payable, accrued expenses, and other liabilities 9,498 4,495
Net cash flows provided by operating activities 22,236 18,825
Net cash flows from investing activities
Capital expenditures (11,188) (9,752)
Payments under Endospan agreements (17,000) (5,000)
Proceeds from sale of non-financial assets, net - 14,250
Net cash flows used in investing activities (28,188) (502)
Net cash flows from financing activities
Proceeds from issuance of long-term debt 184,000 -
Proceeds from revolving credit facility 28,500 -
Repayment of debt (211,831) (2,772)
Proceeds from exercise of stock options and issuance of common stock 5,728 3,955
Payment of debt issuance costs (2,544) (249)
Proceeds from financing insurance premiums - 3,558
Principal payments on short-term notes payable (1,027) (2,531)
Redemption and repurchase of stock to cover tax withholdings - (559)
Other (623) (537)
Net cash flows provided by financing activities 2,203 865
Effect of exchange rate changes on cash and cash equivalents (1,728) 401
(Decrease) increase in cash and cash equivalents (5,477) 19,589
Cash and cash equivalents, beginning of year 58,940 39,351
Cash and cash equivalents, end of year $ 53,463 $ 58,940
Artivion, Inc. and Subsidiaries
Financial Highlights
Three Months Ended December 31, Year Ended December 31,
2024 2023 2024 2023
Products
Aortic stent grafts $ 30,145 $ 27,437 $ 123,081 $ 107,469
On-X 22,178 20,182 83,982 74,528
Surgical sealants 19,935 18,513 73,898 68,016
Other 2,404 3,012 9,269 11,172
Total products 74,662 69,144 290,230 261,185
Preservation services 22,646 24,526 98,307 92,819
Total revenues $ 97,308 $ 93,670 $ 388,537 $ 354,004
North America 49,261 50,062 197,940 187,603
Europe, the Middle East, and Africa 33,362 30,206 131,518 114,814
Asia Pacific 9,574 8,922 37,202 33,577
Latin America 5,111 4,480 21,877 18,010
Total revenues $ 97,308 $ 93,670 $ 388,537 $ 354,004
Artivion, Inc. and Subsidiaries
Reconciliation of GAAP to Non-GAAP
Revenues for the Three Months Ended December 31, Percent Change From Prior Year
2024 2023
US GAAP US GAAP Exchange Rate Effect Constant Currency Constant Currency
Products
Aortic stent grafts $ 30,145 $ 27,437 $ 364 $ 27,801 8%
On-X 22,178 20,182 (6) 20,176 10%
Surgical sealants 19,935 18,513 49 18,562 7%
Other 2,404 3,012 3 3,015 (20)%
Total products 74,662 69,144 410 69,554 7%
Preservation services 22,646 24,526 (7) 24,519 (8) %
Total $ 97,308 $ 93,670 $ 403 $ 94,073 3%
North America 49,261 50,062 (18) 50,044 (2)%
Europe, the Middle East, and Africa 33,362 30,206 844 31,050 7%
Asia Pacific 9,574 8,922 - 8,922 7%
Latin America 5,111 4,480 (423) 4,057 26%
Total $ 97,308 $ 93,670 $ 403 $ 94,073 3%
Revenues for the Year Ended December 31, Percent Change From Prior Year
2024 2023
US GAAP US GAAP Exchange Rate Effect Constant Currency Constant Currency
Products
Aortic stent grafts $ 123,081 107,469 $ 1,052 $ 108,521 13%
On-X 83,982 74,528 (8) 74,520 13%
Surgical sealants 73,898 68,016 39 68,055 9%
Other 9,269 11,172 8 11,180 (17)%
Total products 290,230 261,185 1,091 262,276 11%
Preservation services 98,307 92,819 (34) 92,785 6%
Total $ 388,537 $ 354,004 $ 1,057 $ 355,061 9%
North America 197,940 187,603 (75) 187,528 6%
Europe, the Middle East, and Africa 131,518 114,814 1,838 116,652 13%
Asia Pacific 37,202 33,577 - 33,577 11%
Latin America 21,877 18,010 (706) 17,304 26%
Total $ 388,537 $ 354,004 $ 1,057 $ 355,061 9%
Artivion, Inc. and Subsidiaries
Reconciliation of GAAP to Non-GAAP
General, Administrative, and Marketing Expense, EBITDA, Adjusted EBITDA, and Free Cash Flows
Three Months Ended December 31, Year Ended December 31,
2024 2023 2024 2023
Reconciliation of G A expenses, GAAP to adjusted G A, non-GAAP
General, administrative, and marketing expense, GAAP $ 51,429 $ 50,278 $ 181,455 $ 208,977
Business development, integration, and severance expense (income) 1,297 2,531 (10,626) 24,992
Cybersecurity incident 2,602 - 2,602 -
Corporate rebranding expense - 72 - 355
Abandonment of CardioGenesis cardiac laser therapy business - - - 160
Adjusted G A, non-GAAP $ 47,530 $ 47,675 $ 189,479 $ 183,470
Three Months Ended December 31, Year Ended December 31,
2024 2023 2024 2023
Reconciliation of net loss, GAAP and EBITDA, non-GAAP to adjusted EBITDA, non-GAAP
Net loss, GAAP $ (16,483) $ (3,975) $ (13,359) $ (30,690)
Adjustments
Interest expense 9,742 6,244 34,277 25,299
Interest income (374) (398) (1,467) (1,077)
Income tax (benefit) expense (119) 3,384 5,845 9,104
Depreciation and amortization 6,295 5,816 24,205 23,076
EBITDA, non-GAAP (939) 11,071 49,501 25,712
Non-cash compensation 2,743 3,956 14,242 14,422
Business development, integration, and severance expense (income) 5,821 2,425 (6,102) 29,269
Cybersecurity incident 4,583 - 4,583 -
Loss on extinguishment of debt - - 3,669 -
Loss (gain) on foreign currency revaluation 5,398 (2,192) 5,369 (2,080)
Abandonment of CardioGenesis cardiac laser therapy business - - - 390
Corporate rebranding expense - 72 - 355
Gain from sale of non-financial assets - - - (14,250)
Adjusted EBITDA, non-GAAP $ 17,606 $ 15,332 $ 71,262 $ 53,818
Three Months Ended December 31, Year Ended December 31,
2024 2023 2024 2023
Reconciliation of cash flows from operating activities, GAAP to free cash flows, non-GAAP
Net cash flows provided by operating activities $ 10,139 $ 9,299 $ 22,236 $ 18,825
Capital expenditures (1,425) (2,669) (11,188) (9,752)
Free cash flows, non-GAAP $ 8,714 $ 6,630 $ 11,048 $ 9,073
Artivion Inc. and Subsidiaries
Reconciliation of GAAP to Non-GAAP
Net Income and Diluted Income Per Common Share
In Thousands, Except Per Share Data
Three Months Ended December 31, Year Ended December 31,
2024 2023 2024 2023
GAAP
Loss before income taxes $ (16,602) $ (591) $ (7,514) $ (21,586)
Income tax expense (119) 3,384 5,845 9,104
Net loss $ (16,483) $ (3,975) $ (13,359) $ (30,690)
Diluted loss per common share $ (0.39) $ (0.10) $ (0.32) $ (0.75)
Diluted weighted-average common shares outstanding 41,882 40,898 41,676 40,743
Reconciliation of loss before income taxes, GAAP to adjusted income, non-GAAP
Loss before income taxes, GAAP $ (16,602) $ (591) $ (7,514) $ (21,586)
Adjustments
Amortization expense 4,205 3,745 15,855 15,198
Business development, integration, and severance expense (income) 5,821 2,425 (6,102) 29,269
Non-cash interest expense 2,256 467 3,866 1,858
Cybersecurity incident 4,583 - 4,583 -
Loss on extinguishment of debt - - 3,669 -
Abandonment of CardioGenesis cardiac laser therapy business - - - 390
Corporate rebranding expense - 72 - 355
Gain from sale of non-financial assets - - - (14,250)
Adjusted income before income taxes, non-GAAP 263 6,118 14,357 11,234
Income tax expense calculated at a tax rate of 25% 66 1,529 3,589 2,808
Adjusted net income, non-GAAP $ 197 $ 4,589 $ 10,768 $ 8,426
Reconciliation of diluted loss per common share, GAAP to adjusted diluted income per common share, non-GAAP
Diluted loss per common share, GAAP $ (0.39) $ (0.10) $ (0.32) $ (0.75)
Adjustments
Amortization expense 0.10 0.09 0.37 0.37
Business development, integration, and severance expense (income) 0.14 0.06 (0.14) 0.71
Non-cash interest expense 0.05 0.01 0.09 0.04
Cybersecurity incident 0.11 - 0.11 -
Loss on extinguishment of debt - - 0.09 -
Abandonment of CardioGenesis cardiac laser therapy business - - - 0.01
Corporate rebranding expense - - - 0.01
Gain from sale of non-financial assets - - - (0.34)
Tax effect of non-GAAP adjustments (0.10) (0.03) (0.13) (0.20)
Effect of 25% tax rate 0.09 0.08 0.18 0.35
Adjusted diluted income per common share, non-GAAP $ - $ 0.11 $ 0.25 $ 0.20
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 41,882 40,898 41,676 40,743
Adjustments
Effect of dilutive stock options and awards 1,319 802 1,077 598
Diluted weighted-average common shares outstanding, non-GAAP 43,201 41,700 42,753 41,341

Frequently Asked Questions

What was Artivion's revenue in Q4 2024?

Artivion reported a revenue of $97.3 million in Q4 2024.

How did net loss change in 2024 compared to 2023?

The net loss decreased to $(13.4) million in 2024 from $(30.7) million in 2023.

What is the expected revenue growth for 2025?

Artivion anticipates 2025 revenue growth between 10% and 14%.

What significant FDA approval did Artivion receive?

Artivion received a Humanitarian Device Exemption for the AMDS Hybrid Prosthesis.

What was the adjusted EBITDA for Q4 2024?

Adjusted EBITDA for Q4 2024 was $17.6 million, up 15% from Q4 2023.

Last updated: Feb 24, 2025