AORT

Artivion Inc
NYSEHEALTHCAREMEDICAL DEVICES

Key Statistics

Market Cap
$1.19B
P/E Ratio
97.84
EPS
$0.25
Beta
1.25
52W High
$48.25
52W Low
$19.16
50-Day MA
$24.91
200-Day MA
$37.29
Dividend Yield
Profit Margin
2.55%
Forward P/E
149.25
PEG Ratio
643.75

About Artivion Inc

Artivion Inc. manufactures, processes and distributes implantable human tissues and medical devices worldwide.

Official WebsiteUSAFY End: December

Fundamentals

Revenue (TTM)$458.69M
Gross Profit (TTM)$296.10M
EBITDA$61.40M
Operating Margin5.18%
Return on Equity3.14%
Return on Assets2.84%
Revenue/Share (TTM)$9.80
Book Value$9.29
Price-to-Book2.58
Price-to-Sales (TTM)2.59
EV/Revenue2.978
EV/EBITDA21.00
Quarterly Earnings Growth (YoY)0.00%
Quarterly Revenue Growth (YoY)17.50%
Shares Outstanding$48.54M
Float$45.97M
% Insiders4.49%
% Institutions92.84%

Historical Volatility

HV 10-Day
58.73%
HV 20-Day
52.30%
HV 30-Day
49.91%
HV 60-Day
82.71%
HV Rank
76.2%

Volatility is currently expanding

Analyst Ratings

Consensus ($42.00 target)
2
Strong Buy
6
Buy

Latest News

Artivion: PMA Approval Supports Accelerating Growth And Margin Expansion

Artivion benefits from FDA premarket approval of AMDS, removing adoption barriers and unlocking a $150M U.S. TAM in acute aortic dissection. AMDS's clinical data shows reduced mortality and major adverse events, with the elimination of DANE tears and durable benefit, supporting rapid, adoption-driven commercial scaling. AORT demonstrates double-digit revenue growth, margin expansion, and a shift to GAAP profitability, with EBITDA up 26% and gross margins nearing 65%.

Seeking Alpha6/30/2026Positive
Artivion Announces U.S. FDA Approval of the AMDS Hybrid Prosthesis

ATLANTA, June 29, 2026 /PRNewswire/ -- Artivion, Inc. (NYSE: AORT), a leading cardiac and vascular surgery company focused on aortic disease, today announced that the U.S. Food and Drug Administration (FDA) has approved the premarket approval application (PMA) for the AMDS Hybrid Prosthesis ("AMDS"). The approval covers acute Debakey Type I aortic dissections with either clinical or radiographic malperfusion, which the Company estimates to be approximately 60% of all Debakey Type I aortic dissections.

PRNewsWire6/29/2026Neutral
Artivion to Participate in the 2026 Truist Securities MedTech Conference

ATLANTA, June 10, 2026 /PRNewswire/ -- Artivion, Inc. (NYSE: AORT), a leading cardiac and vascular surgery company focused on aortic disease, announced today that it will participate at the upcoming 2026 Truist Securities MedTech Conference on Tuesday, June 16, 2026, at the Boston Harbor Hotel. The Company's fireside chat is scheduled to begin at 1:00 p.m.

PRNewsWire6/10/2026Neutral
Artivion Completes Acquisition of Endospan Ltd.

ATLANTA, May 18, 2026 Artivion, Inc. (NYSE: AORT), a leading cardiac and vascular surgery company focused on aortic disease, today announced that it has completed the acquisition of its long-standing partner Endospan Ltd. ("Endospan"), a pioneer in the endovascular repair of aortic arch disease  and developer of the NEXUS® Aortic Arch System.

PRNewsWire5/18/2026Neutral
Artivion Reports First Quarter 2026 Financial Results and Announces Exercise of Option to Acquire Endospan

First Quarter & Recent Business Highlights: Achieved revenue of $116.3 million in the first quarter of 2026 versus $99.0 million in the first quarter of 2025, an increase of 18% on a GAAP basis and 12% on a non-GAAP constant currency basis  Net income for the first quarter of 2026 was $1.4 million, or $0.03 per fully diluted share, and non-GAAP net income was $4.2 million, or $0.08 per fully diluted share Adjusted EBITDA increased 26% to $22.1 million in the first quarter of 2026 compared to $17.5 million in the first quarter of 2025 Announced U.S. FDA PMA Approval of the NEXUS Aortic Arch System for the treatment of aortic arch disease, including chronic aortic dissections Exercised option to acquire Endospan for an upfront purchase price of $135 million, net of previously extended loans ATLANTA, May 7, 2026 /PRNewswire/ -- Artivion, Inc. (NYSE: AORT), a leading cardiac and vascular surgery company focused on aortic disease, today announced financial results for the first quarter ended March 31, 2026. "In the first quarter of 2026, we achieved 12% constant currency revenue growth and 26% adjusted EBITDA growth, reflecting continued execution of our strategy to deliver long-term, profitable performance with an expanding and clinically differentiated product portfolio.

PRNewsWire5/7/2026Neutral

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Data last updated: 7/9/2026