Vita Zahnfabrik GmbH H Rauter & CO
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 3
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K211854 | VITA Akzent LC | November 22, 2021 |
| K193434 | VITA LUMEX AC | July 21, 2020 |
| K193436 | VITA Ambria | May 14, 2020 |