Artivion, Inc.

Artivion, Inc.

CRY
Artivion, Inc.US flagNew York Stock Exchange
17.88
USD
+0.25
- -
725.15MMarket Cap
No data availableFinancial data will appear here once available

Capital Structure

FRC

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Working Capital

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Growth Rates

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Quarterly Revenue

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Quarterly Earnings Per Share

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Quarterly Dividends Per Share

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Company Description

APIChat
CEO
James Mackin
Full Time Employees
1,200
Sector
Healthcare
Industry
Medical - Devices
Address
1655 Roberts Blvd NW Kennesaw GA United States of America 30144
IPO Date
Feb 12, 1993
Business
Artivion, Inc. (NYSE: AORT; formerly CryoLife, Inc.) manufactures, processes and distributes medical devices and implantable tissues for cardiac and vascular surgical procedures, with a focus on the treatment of aortic diseases; core products and services include aortic stent grafts such as NEXUS®, NEXUS DUO™, NEXUS TRE™, E-vita® Open Neo, Neo EDE™, E-xtra Design MultiBranch, E-nside™ TAAA, Artivex™ and abdominal/peripheral aorta stent grafts; On-X® mechanical heart valves and surgical products; surgical sealants including BioGlue®; cryopreserved human tissue allografts such as CryoVein®, CryoArtery®, CryoPatch® SG, CryoGraft® and PhotoFix®; and ancillary solutions like CarbonAid®, E-wire guidewires and E-xpand balloon catheters. Founded in 1984 and headquartered in Kennesaw, Georgia, the company operates globally with manufacturing, sales and distribution in the United States, Europe, Asia Pacific, Latin America and other regions, serving cardiac, vascular and thoracic surgeons, hospitals and healthcare facilities. Recent developments include amended funding and purchase option terms with Endospan Ltd. in 2024 for up to $25 million in additional loans and a reduced upfront acquisition price to $175 million for the NEXUS Stent Graft System pending U.S. FDA approval; $350 million in credit facilities from Ares Management in January 2024 comprising a $190 million term loan, $100 million delayed draw term loan and $60 million revolver; the exchange of $99.5 million in 4.25% convertible senior notes due 2025 for common stock in May 2025; FDA IDE approval for the ARTIZEN pivotal trial of the Arcevo LSA device; positive clinical data from AMDS PERSEVERE and PROTECT trials presented in 2025 supporting premarket approval for acute aortic dissection treatment; and launches including AMDS with U.S. PMA approval in late 2024 and ongoing expansions in On-X valves, stent grafts and geographic markets like Asia Pacific and Latin America, driving reported revenue growth and raised 2024-2025 guidance.

Company News

APIChat
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  • Artivion, Inc. (AORT) Q2 2024 Earnings Call Transcript

  • Artivion (AORT) Surpasses Q2 Earnings and Revenue Estimates

  • Artivion Reports Second Quarter 2024 Financial Results

  • Artivion to Participate in Upcoming Investor Conferences

  • Artivion Announces Release Date and Teleconference Call Details for Second Quarter 2024 Financial Results

  • Artivion Amends Agreements with Endospan

  • Data-Driven Growth Fuels More Upside For Overlooked Artivion

  • Artivion Obtains $350 Million in Senior Secured Credit Facilities

  • Artivion Announces FDA PMA Approval of PerClot and Transfer of PMA to Baxter

  • A Trio of Low Price-Sales Ratio Stocks

  • Wall Street Analysts Think CryoLife (CRY) Could Surge 51%: Read This Before Placing a Bet

  • CryoLife, Inc. (CRY) CEO J. Patrick Mackin on Q3 2021 Results - Earnings Call Transcript

  • Recap: Cryolife Q3 Earnings

  • Anthony Semedo Joins CryoLife Board of Directors

  • CryoLife to Participate in the Morgan Stanley 19th Annual Global Healthcare Conference

  • CryoLife, Inc. (CRY) CEO Pat Mackin on Q2 2021 Results - Earnings Call Transcript

  • CryoLife (CRY) Reports Q2 Loss, Tops Revenue Estimates