Denmat Holding, LLC
FDA 510(k) & PMA Approved Devices — 2 products
Total Devices2
Categories2
Latest FDA decision2025-08-25
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K251593 | DenMat Multilayered Zirconia Disc | EIH | 2025-08-25 | View |
| 510(k) | K222357 | DenMat Glutaraldehyde Desensitizer | KLE | 2022-08-09 | View |
No matching devices.