Estelite Color 10917
by Tokuyama Dental Corporation
Estelite Color 10917 is a Class II device made by Tokuyama Dental Corporation, cleared under FDA 510(k) K110178 on 5 Apr 2011 and listed in FDA GUDID since 23 Sep 2016 (UDI-DI 04548190109173), active as of 23 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 | Number04548190109173 | Date23 Sep 2016 | StatusListed |
| United States | FDA 510(k)SESE | NumberK110178 | Date5 Apr 2011 | StatusActive |
Official records
- AccessGUDID record 04548190109173
- FDA 510(k) database K110178
Across registries
- FDA 510(k) K110178 decided 5 Apr 2011 Active
- FDA GUDID UDI-DI 04548190109173 listed 23 Sep 2016 Listed
Timeline
- Cleared FDA 510(k) K110178
- Listed FDA GUDID 04548190109173
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Estelite Color
- Generic name
- Dental composite resin
- Model / reference
- 10917
- Primary DI / UDI-DI
- 04548190109173
- 510(k) Number
- FDA product code
- EBF
- GMDN term
- Dental composite resin
- Device class
- Class II
- Regulation number
- 872.3690
- GUDID distribution status
- In Commercial Distribution
Similar devices in this category
Other devices filed under Dental composite resin.
- Simile N56BP by KERR CORPORATION
- Harvard Temp Cem 7081100 by Harvard Dental International GmbH
- DiaFil Flow Refill Pacakge A2O A2001-4208 by DiaDent Group International
- DiaFil Flow Refill Package B3 A2001-4206 by DiaDent Group International
- TPH Spectra ST flow 642532 by Dentsply De Trey GmbH
- Simile N56AD by KERR CORPORATION
- Nexcomp flow C2 9253 by Meta Biomed Co., Ltd.
- Nexcomp flow OA3 9256 by Meta Biomed Co., Ltd.
- Natural Elegance Bulk Fill 5722807 by CB Dental Reg. GmbH
- SYNERGY 7833 by Coltène/Whaledent AG