Gradia® 001422
Gradia® 001422 is a Class II device made by Gc America Inc., cleared under FDA 510(k) K001518 on 5 Jul 2000 and listed in FDA GUDID since 1 Aug 2016 (UDI-DI D0470014221), 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 | NumberD0470014221 | Date1 Aug 2016 | StatusListed |
| United States | FDA 510(k)SESE | NumberK001518 | Date5 Jul 2000 | StatusActive |
Official records
- FDA 510(k) database K001518
Across registries
- FDA 510(k) K001518 decided 5 Jul 2000 Active
- FDA GUDID UDI-DI D0470014221 listed 1 Aug 2016 Listed
Timeline
- Cleared FDA 510(k) K001518
- Listed FDA GUDID D0470014221
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Gradia®
- Generic name
- Light-cured dental restorative composite resin
- Model / Ref / Catalog
- 001422
- Primary DI / UDI-DI
- D0470014221
- 510(k) Number
- FDA product code
- EBF
- GMDN term
- Light-cured dental restorative composite resin
- Device class
- Class II
- Regulation number
- 872.3690
- GUDID distribution status
- In Commercial Distribution
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