W&H Dentalwerk Buermoss GmbH
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 2
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K223173 | Proxeo ULTRA (PB-510, PB-520 and PB-530) | July 14, 2023 |
| K213221 | AMADEO, M-UK1015 (incl. attachments and accessories) | May 26, 2022 |