Restor3D, Inc.
FDA 510(k) & PMA Approved Devices — 6 products
Total Devices6
Categories6
Latest FDA decision2025-12-05
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K252067 | Velora Acetabular System | LPH | 2025-12-05 | View |
| 510(k) | K243768 | iTotal® Identity™ Cruciate Retaining 3DP Porous Knee Replacement System | MBH | 2025-03-27 | View |
| 510(k) | K242356 | TIDAL Fusion Cage System | SAI | 2025-03-24 | View |
| 510(k) | K240591 | restor3d Kinos Axiom Total Ankle System | HSN | 2024-04-29 | View |
| 510(k) | K201393 | restor3d MTP Implant | KWD | 2022-05-25 | View |
| 510(k) | K201314 | Restor3d Utility Wedge | PLF | 2021-06-17 | View |
No matching devices.