Master-Dent 19-412-A3.5
Master-Dent 19-412-A3.5 is a device made by Dentonics, Inc., cleared under FDA 510(k) K833810 on 21 Feb 1984 and listed in FDA GUDID since 23 Sep 2016 (UDI-DI 00816526021500), active as of 22 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00816526021500 | Date23 Sep 2016 | StatusListed |
| United States | FDA 510(k)SESE | NumberK833810 | Date21 Feb 1984 | StatusActive |
Official records
- AccessGUDID record 00816526021500
- FDA 510(k) database K833810
Across registries
- FDA 510(k) K833810 decided 21 Feb 1984 Active
- FDA GUDID UDI-DI 00816526021500 listed 23 Sep 2016 Listed
Timeline
- Cleared FDA 510(k) K833810
- Listed FDA GUDID 00816526021500
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Master-Dent
- Generic name
- Dental composite resin
- Model / reference
- 19-412-A3.5
- Primary DI / UDI-DI
- 00816526021500
- 510(k) Number
- GMDN term
- Dental composite resin
- GUDID distribution status
- In Commercial Distribution
Similar devices in this category
Other devices filed under Dental composite resin.
- Admira Flow 2486 by VOCO GmbH
- Rebilda Post 1771 by VOCO GmbH
- DenFil DF205-RB33 by VERICOM CO., LTD.
- REFLECTYS B2 CP CPTYS-B2 by ITENA CLINICAL
- REFLECTYS A4 CP CPTYS-A4 by ITENA CLINICAL
- BRILLIANT Flow 7101 by Coltène/Whaledent AG
- TPH Spectra ST flow 642527 by Dentsply De Trey GmbH
- Simile N56BO by KERR CORPORATION
- Flow-It ALC N11K by KERR CORPORATION
- SYNERGY D6 8376 by Coltène/Whaledent AG