Prevest Denpro Limited
FDA 510(k) & PMA Approved Devices — 7 products
Total Devices7
Categories6
Latest FDA decision2024-11-27
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K233273 | C&B Ceramic; C&B Permanent; C&B Interim | EBF | 2024-11-27 | View |
| 510(k) | K231263 | Fusion Core DC Flo; Fusion Flo; Fusion Flo SE; Fusion 1 Seal; Magna NT | EBF | 2024-01-05 | View |
| 510(k) | K231696 | Fusion Bond 5, Fusion Bond 7, Fusion Bond DC, Renew MDP, Renew Universal | KLE | 2023-08-11 | View |
| 510(k) | K213244 | Accusil Dental Impression Materials (Accusil Light Body Regular and Fast Set, Accusil Heavy Body Regular and Fast Set, Accusil Monophase Regular and Fast Set, Accusil Putty Regular and Fast Set, Accusil Bite Registration) | ELW | 2022-09-09 | View |
| 510(k) | K212563 | CalApex Calplus, Cerafill RCS, Endoseal, Nanoseal S, Zical Ultra Paste, Zical Ultra Powder/Liquid | KIF | 2022-05-23 | View |
| 510(k) | K212475 | Prevest Denpro Cavity Liners (Apacal ART, Cal LC, Calcigel, CalUltra) | EJK | 2022-05-13 | View |
| 510(k) | K200555 | Prevest Denpro Dental Cements (Micron Bioactive, Micron Superior, Micron Superior Capsules, Micron Luting, Micron Dentin Conditioner) | EMA | 2021-05-13 | View |
No matching devices.