G-aenial™ 012395
G-aenial™ 012395 is a Class II device made by Gc America Inc., cleared under FDA 510(k) K173500 on 8 Mar 2018 and listed in FDA GUDID since 1 Oct 2018 (UDI-DI D0470123951), 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 | NumberD0470123951 | Date1 Oct 2018 | StatusListed |
| United States | FDA 510(k)SESE | NumberK173500 | Date8 Mar 2018 | StatusActive |
Official records
- FDA 510(k) database K173500
Across registries
- FDA 510(k) K173500 decided 8 Mar 2018 Active
- FDA GUDID UDI-DI D0470123951 listed 1 Oct 2018 Listed
Timeline
- Cleared FDA 510(k) K173500
- Listed FDA GUDID D0470123951
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- G-aenial™
- Generic name
- Dental composite resin
- Model / Ref / Catalog
- 012395
- Primary DI / UDI-DI
- D0470123951
- 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
- Size
- Total Volume — 2 Milliliter
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