Reprise Biomedical, Inc.
FDA 510(k) & PMA Approved Devices — 4 products
Total Devices4
Categories1
Latest FDA decision2024-04-19
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K240753 | Miro3D Fibers Wound Matrix | KGN | 2024-04-19 | View |
| 510(k) | K240277 | MiroDry Wound Matrix | KGN | 2024-03-01 | View |
| 510(k) | K231614 | MiroTract Wound Matrix | KGN | 2023-12-13 | View |
| 510(k) | K221520 | Miro3D Wound Matrix | KGN | 2022-08-18 | View |
No matching devices.