Prosidyan, Inc.
FDA 510(k) & PMA Approved Devices — 8 products
Total Devices8
Categories2
Latest Approval2025-10-22
| Type | Number | Device Name | Code | Date | |
|---|---|---|---|---|---|
| 510(k) | K253147 | FIBERGRAFT BG Putty GPS Bone Graft Substitute FIBERGRAFT BG Putty Bone Graft Substitute FIBERGRAFT AERIDYAN Matrix Bone Graft Substitute FIBERGRAFT BG Matrix Bone Graft Substitute | MQV | 2025-10-22 | View |
| 510(k) | K251648 | GPS Advanced; GPS Advanced Cannula | FMF | 2025-06-24 | View |
| 510(k) | K241426 | GPS Advanced; 5 cc GPS Advanced Cannula | FMF | 2024-07-10 | View |
| 510(k) | K213803 | FIBERGRAFT Aeridyan Matrix Bone Graft Substitute | MQV | 2022-08-23 | View |
| 510(k) | K182670 | FIBERGRAFT AERIDYAN Matrix Bone Graft Substitute | MQV | 2018-12-20 | View |
| 510(k) | K180080 | FIBERGRAFT BG Matrix Bone Graft Substitute | MQV | 2018-04-06 | View |
| 510(k) | K171284 | FIBERGRAFT BG Matrix Bone Graft Substitute | MQV | 2017-06-30 | View |
| 510(k) | K170306 | FIBERGRAFT BG Putty Bone Graft Substitute | MQV | 2017-05-24 | View |
No matching devices.