Forest 9083G
Forest 9083G is a Class I device made by Ls Enterprises, Inc., listed in FDA GUDID since 8 Dec 2022 (UDI-DI D0699083G0), registry data as of 22 Oct 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | NumberD0699083G0 | Date8 Dec 2022 | StatusListed |
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Forest
- Generic name
- Operating room light
- Model / reference
- 9083G
- Primary DI / UDI-DI
- D0699083G0
- FDA product code
- EAZ
- GMDN term
- Operating room light
- Device class
- Class I
- Regulation number
- 872.4630
- GUDID distribution status
- In Commercial Distribution
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