Artivion, Inc.
FDA 510(k) & PMA Approved Devices — 2 products
Total Devices2
Categories2
Latest FDA decision2026-06-26
SEC Filings: 1 filings on record. Latest: 10-Q (2026-08-07). View on SEC EDGAR →
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| PMA | P250055 | Hybrid stent graft, thoracic aortic lesion treatment | QSK | 2026-06-26 | View |
| 510(k) | K252059 | CryoValve SG Pulmonary Valve (SGPV10) CryoValve SG Pulmonary Valve and Conduit (SGPV00) | OHA | 2025-10-02 | View |
No matching devices.