W&H Dentalwerk Buermoss GmbH
FDA 510(k) & PMA Approved Devices — 2 products
Total Devices2
Categories2
Latest FDA decision2023-07-14
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K223173 | Proxeo ULTRA (PB-510, PB-520 and PB-530) | ELC | 2023-07-14 | View |
| 510(k) | K213221 | AMADEO, M-UK1015 (incl. attachments and accessories) | ERL | 2022-05-26 | View |
No matching devices.