Forest 4987FE-G
Forest 4987FE-G is a Class I device made by Ls Enterprises, Inc., cleared under FDA 510(k) K173608 on 17 Aug 2018 and listed in FDA GUDID since 7 Dec 2022 (UDI-DI D0694987FEG0), 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 | NumberD0694987FEG0 | Date7 Dec 2022 | StatusListed |
| United States | FDA 510(k)SESE | NumberK173608 | Date17 Aug 2018 | StatusActive |
Official records
- FDA 510(k) database K173608
Across registries
- FDA 510(k) K173608 decided 17 Aug 2018 Active
- FDA GUDID UDI-DI D0694987FEG0 listed 7 Dec 2022 Listed
Timeline
- Cleared FDA 510(k) K173608
- Listed FDA GUDID D0694987FEG0
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Forest
- Generic name
- Dental delivery system
- Model / reference
- 4987FE-G
- Primary DI / UDI-DI
- D0694987FEG0
- 510(k) Number
- FDA product code
- EIA
- GMDN term
- Dental delivery system
- Device class
- Class I
- Regulation number
- 872.6640
- GUDID distribution status
- In Commercial Distribution
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