Organogenesis, Inc.
FDA 510(k) & PMA Approved Devices — 2 products
Total Devices2
Categories1
Latest FDA decision2023-05-02
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K212579 | FortiShield (Biosynthetic Wound Matrix) | KGN | 2023-05-02 | View |
| 510(k) | K220317 | PuraPly Micronized Wound Matrix (PuraPly MZ) | KGN | 2022-07-01 | View |
No matching devices.