Synovis Life Technologies, Inc.
FDA 510(k) & PMA Approved Devices — 3 products
Total Devices3
Categories2
Latest Approval2023-04-07
| Type | Number | Device Name | Code | Date | |
|---|---|---|---|---|---|
| 510(k) | K223052 | Peri-Guard and Supple Peri-Guard | FTM | 2023-04-07 | View |
| 510(k) | K221029 | PERI-GUARD Repair Patch, SUPPLE PERI-GUARD Repair Patch | PSQ | 2022-10-19 | View |
| 510(k) | K221032 | Vascu-Guard Vascular Repair Patch | PSQ | 2022-10-19 | View |
No matching devices.