Brilliant Ng 1220
Brilliant Ng 1220 is a Class II device made by Coltène/Whaledent AG, cleared under FDA 510(k) K974465 on 9 Mar 1998 and listed in FDA GUDID since 1 Sep 2016 (UDI-DI J00612200), 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 | NumberJ00612200 | Date1 Sep 2016 | StatusListed |
| United States | FDA 510(k)SESE | NumberK974465 | Date9 Mar 1998 | StatusActive |
Official records
- FDA 510(k) database K974465
Across registries
- FDA 510(k) K974465 decided 9 Mar 1998 Active
- FDA GUDID UDI-DI J00612200 listed 1 Sep 2016 Listed
Timeline
- Cleared FDA 510(k) K974465
- Listed FDA GUDID J00612200
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Brilliant Ng
- Generic name
- Dental veneer, professional
- Model / Ref / Catalog
- 1220
- Primary DI / UDI-DI
- J00612200
- 510(k) Number
- FDA product code
- EBF
- GMDN term
- Dental veneer, professional
- Device class
- Class II
- Regulation number
- 872.3690
- GUDID distribution status
- In Commercial Distribution
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