Changzhou Bomedent Medical Technology Co.,Ltd
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 3
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K213947 | Ultrasonic Endo Activation Device (Model:Actor I pro) | September 8, 2022 |
| K203836 | BOMEDENT Apex locator, WISMY Apex locator | March 30, 2021 |
| K191276 | Dental Electrical Motor iRoot Pro | June 30, 2020 |