Changzhou Bomedent Medical Technology Co.,Ltd
FDA 510(k) & PMA Approved Devices — 3 products
Total Devices3
Categories3
Latest FDA decision2022-09-08
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K213947 | Ultrasonic Endo Activation Device (Model:Actor I pro) | ELC | 2022-09-08 | View |
| 510(k) | K203836 | BOMEDENT Apex locator, WISMY Apex locator | LQY | 2021-03-30 | View |
| 510(k) | K191276 | Dental Electrical Motor iRoot Pro | EKX | 2020-06-30 | View |
No matching devices.