Dmp Dental Industry S.A.
FDA 510(k) & PMA Approved Devices — 3 products
Total Devices3
Categories3
Latest Approval2026-01-13
| Type | Number | Device Name | Code | Date | |
|---|---|---|---|---|---|
| 510(k) | K253248 | Bright Cavity Liner | EJK | 2026-01-13 | View |
| 510(k) | K252469 | MAGNABOND SE; MAGNABOND UNIVERSAL; MAGNABOND UNIVERSAL DCA | KLE | 2025-11-06 | View |
| 510(k) | K192830 | Bright Temporary C&B | EBG | 2020-09-02 | View |
No matching devices.