ARTIVION INC

Insider Trading & Executive Data

AORT
NYSE
Healthcare
Medical Devices

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136 insider trades in the last year. Go beyond summary counts with transaction-level detail, compensation intelligence, and institutional ownership context.

Trade-level insider transactions with filing links, transaction codes, and footnotes
Executive compensation trends by role with year-over-year comparisons
Institutional ownership shifts by quarter with top-holder concentration data
Form 144 and Form 8-K monitoring with AI analysis and CSV export tools

Insider Activity Summary

Insider Trades (1Y)
136
17 in last 30 days
Buy / Sell (1Y)
45/91
Acquisitions / Dispositions
Unique Insiders (1Y)
14
Active in past year
Insider Positions
24
Current holdings
Position Status
19/5
Active / Exited
Institutional Holders
217
Latest quarter
Board Members
25

Compensation & Governance

Avg Total Compensation
$2.0M
Latest year: 2024
Executives Covered
8
Comp records available
Form 8-K Events (1Y)
1
Personnel Changes (1Y)
1
Bonus Plan Events (1Y)
0
Organization Changes (1Y)
0
Board Appointments (1Y)
1
Board Departures (1Y)
1

Restricted Sales

Form 144 Filings (1Y)
53
Form 144 Insiders (1Y)
8
Planned Sale Shares (1Y)
601.7K
Planned Sale Value (1Y)
$23.0M
Price
$38.27
Market Cap
$1.8B
Volume
14,401.84
EPS
$0.21
Revenue
$441.3M
Employees
1.6K
About ARTIVION INC

Company Overview

Artivion, Inc. (NYSE: AORT) is a specialty medical device and human-tissue preservation company focused on aortic and cardiac surgical solutions, selling aortic stent grafts, surgical sealants (BioGlue), On‑X mechanical valves and preserved human cardiac/vascular tissues. Revenue is reported across Medical Devices and Preservation Services and is driven by global direct sales and distributor channels, with key manufacturing and tissue‑processing sites in the U.S. and Germany. The company invests meaningfully in R&D (~$28.5M in 2024, ~7% of revenues), runs clinical programs (AMDS with FDA HDE and ongoing PMA pathway) and faces heavy regulatory oversight, tissue‑supply constraints and single‑source supplier risks. Recent financials show mid‑single‑digit to double‑digit top‑line growth (2024 revenue $388.5M) but leverage, interest expense and a 2024 net loss have pressured net results and liquidity.

Executive Compensation Practices

Compensation is likely structured around a typical medical‑device mix of base salary, annual bonuses tied to sales/volume and margin targets, and equity‑based long‑term incentives aimed at aligning management with clinical and regulatory milestones (e.g., PMA approval for AMDS) and market‑share gains for On‑X and stent grafts. Company disclosures show rising stock‑based compensation and contingent‑consideration accounting swings that materially affect G&A, so equity and milestone‑linked pay are likely significant drivers for executives. Given material indebtedness and liquidity management (convertible notes, revolver availability, contingent payments from acquisitions), bonus and LTIP metrics may incorporate cash flow, debt reduction/refinancing outcomes, and successful integration/contingent milestone achievement. The firm’s operational reliance on tissue yield, EtO sterilization capacity, and supplier continuity likely favors retention/vesting provisions and special grants to retain commercial and technical talent who drive adoption and surgeon training.

Insider Trading Considerations

Insider trading patterns at Artivion will likely cluster around binary regulatory and clinical events (PMA/HDE milestones for AMDS and other breakthrough‑designated devices), quarterly earnings that reflect tissue backlog releases and seasonality, and financing actions (convertible note conversions, debt refinancing, or contingent payment milestones). Management has recently shown increases in stock‑based comp and executed a conversion of convertible notes into equity, events that commonly change insider ownership profiles and may prompt preplanned sales for tax/liquidity needs; watch for Rule 10b5‑1 plan filings and Section 16 reporting. Regulatory sensitivities (FDA device classifications, human tissue rules and potential reclassification of allografts), cyberincident disclosures, and supplier or donor‑supply shocks create event risk that can trigger opportunistic insider buys or sells; usual healthcare blackout periods and insider‑reporting rules will apply, so verify timing relative to known clinical/regulatory windows.

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