Promethean Restorative, LLC
FDA 510(k) & PMA Approved Devices — 3 products
Total Devices3
Categories2
Latest Approval2026-01-12
| Type | Number | Device Name | Code | Date | |
|---|---|---|---|---|---|
| 510(k) | K252962 | DYNAMIS Navigation System | OLO | 2026-01-12 | View |
| 510(k) | K251075 | DYNAMIS Implant System | OUR | 2025-04-25 | View |
| 510(k) | K243565 | DYNAMIS SI Screw System | OUR | 2025-02-28 | View |
No matching devices.