DiaDent Group International
DiaDent Group International appears in FDA public data with 0 recalls, 24 510(k) clearances, 1 FDA inspection, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on September 16, 2026.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 24
- Inspections
- 1
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K254152 | Dia-X Sil Light Body | September 16, 2026 |
| K254142 | Dia-X Sil Heavy Body | September 16, 2026 |
| K261166 | DIA-CEM | July 9, 2026 |
| K261093 | DIAFIL | June 2, 2026 |
| K261071 | DIAFIL Bulk FLOW (Economic Package);DIAFIL Bulk FLOW (Refill Package);DIAFIL Bulk FLOW (0.5g) | May 19, 2026 |
| K254112 | Dia-X Sil Bite | March 19, 2026 |
| K231552 | Dia-Cem | July 28, 2023 |
| K220804 | Dia-X Bond Universal | June 15, 2022 |
| K213401 | DIAPLUS Universal | January 31, 2022 |
| K210421 | Diafil & Diafil Capsule | June 28, 2021 |
| K210333 | DiaPaste | March 25, 2021 |
| K200174 | DIA-ROOT BIO MTA | September 18, 2020 |
| K200809 | D-LUX+ | August 7, 2020 |
| K200175 | DIA-ROOT BIO Sealer | June 25, 2020 |
| K192392 | DiaPlus | May 26, 2020 |
| K190091 | Diapaste | March 27, 2020 |
| K192284 | DiaFil Flow | March 25, 2020 |
| K192510 | DIAFIL & DIAFIL Capsule | March 20, 2020 |
| K192022 | DiaTemp Flow | February 13, 2020 |
| K192158 | DiaTemp | February 13, 2020 |