Datum Dental, Ltd.
FDA 510(k) & PMA Approved Devices — 4 products
Total Devices4
Categories2
Latest FDA decision2022-07-18
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K212509 | OSSIX Breeze | NPL | 2022-07-18 | View |
| 510(k) | K163714 | OSSIX BONE | NPM | 2017-07-18 | View |
| 510(k) | K160281 | OSSIX PLUS | NPL | 2016-08-04 | View |
| 510(k) | K153549 | OSSIX VOLUMAX | NPL | 2016-08-04 | View |
No matching devices.