DiaDent Group International
FDA 510(k) & PMA Approved Dispositivos — 23 products
Publicidade
Total de dispositivos23
Categorias0
Última decisão da FDA
| Tipo | Número | Nome do dispositivo | Código | Data | Ações |
|---|---|---|---|---|---|
| 510(k) | K254152 | Dia-X Sil Light Body | ELW | 2026-09-16 | Ver |
| 510(k) | K254142 | Dia-X Sil Heavy Body | ELW | 2026-09-16 | Ver |
| 510(k) | K261166 | DIA-CEM | EMA | 2026-07-09 | Ver |
| 510(k) | K261093 | DIAFIL | EBF | 2026-06-02 | Ver |
| 510(k) | K261071 | DIAFIL Bulk FLOW (Economic Package);DIAFIL Bulk FLOW (Refill Package);DIAFIL Bulk FLOW (0.5g) | EBF | 2026-05-19 | Ver |
| 510(k) | K254112 | Dia-X Sil Bite | ELW | 2026-03-19 | Ver |
| 510(k) | K231552 | Dia-Cem | EMA | 2023-07-28 | Ver |
| 510(k) | K220804 | Dia-X Bond Universal | KLE | 2022-06-15 | Ver |
| 510(k) | K213401 | DIAPLUS Universal | KLE | 2022-01-31 | Ver |
| 510(k) | K210421 | Diafil & Diafil Capsule | EBF | 2021-06-28 | Ver |
| 510(k) | K210333 | DiaPaste | KIF | 2021-03-25 | Ver |
| 510(k) | K200174 | DIA-ROOT BIO MTA | KIF | 2020-09-18 | Ver |
| 510(k) | K200809 | D-LUX+ | EBZ | 2020-08-07 | Ver |
| 510(k) | K200175 | DIA-ROOT BIO Sealer | KIF | 2020-06-25 | Ver |
| 510(k) | K192392 | DiaPlus | KLE | 2020-05-26 | Ver |
| 510(k) | K190091 | Diapaste | KIF | 2020-03-27 | Ver |
| 510(k) | K192284 | DiaFil Flow | EBF | 2020-03-25 | Ver |
| 510(k) | K192510 | DIAFIL & DIAFIL Capsule | EBF | 2020-03-20 | Ver |
| 510(k) | K192022 | DiaTemp Flow | EBG | 2020-02-13 | Ver |
| 510(k) | K192158 | DiaTemp | EBG | 2020-02-13 | Ver |
Nenhum dispositivo correspondente.