DiaDent Group International
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 18
- Inspections
- 1
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| 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 |
| K192273 | DIAETCH Economic Package Type A, DIATECH Regular Package, DIAETCH Refill Package Type A, DIAETCH Int | February 7, 2020 |
| K182009 | Dia-Proseal | September 26, 2019 |
| K182625 | Diapex Plus | June 3, 2019 |
| K130163 | D-LUX | August 16, 2013 |