Restor3D
FDA 510(k) & PMA Approved Devices — 13 products
Total Devices13
Categories7
Latest FDA decision2026-07-01
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K260556 | Veritas Shoulder System | PHX | 2026-07-01 | View |
| 510(k) | K253992 | Veritas Reverse Total Shoulder System | PHX | 2026-05-07 | View |
| 510(k) | K252454 | Kinos Total Ankle System | HSN | 2025-09-03 | View |
| 510(k) | K243643 | restor3d Reverse Total Shoulder Arthroplasty System | PHX | 2025-05-19 | View |
| 510(k) | K242868 | Kinos Total Ankle System | HSN | 2024-10-18 | View |
| 510(k) | K241482 | Kinos Total Ankle System | HSN | 2024-07-22 | View |
| 510(k) | K234087 | restor3d TIDAL Lumbar Interbody Fusion System | MAX | 2024-01-22 | View |
| 510(k) | K232595 | Kinos Axiom Total Ankle System | HSN | 2023-11-28 | View |
| 510(k) | K231458 | Extremity Staple | JDR | 2023-08-03 | View |
| 510(k) | K223326 | Axiom PSR System | OYK | 2023-03-30 | View |
| 510(k) | K220523 | restor3d TiDAL Lumbar Interbody Fusion Device | MAX | 2022-06-17 | View |
| 510(k) | K211789 | restor3d Pin Implants | HTY | 2022-01-04 | View |
| 510(k) | K193491 | restor3d Metallic Interference Screw | HWC | 2020-03-19 | View |
No matching devices.