Forest 2500
Forest 2500 is a dental delivery system (FDA Class I; FDA product code EIA, Unit, Operative Dental) 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 D06925000), 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 | NumberD06925000 | 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 D06925000 listed 7 Dec 2022 Listed
Timeline
- Cleared FDA 510(k) K173608
- Listed FDA GUDID D06925000
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Forest
- Generic name
- Dental delivery system
- Model / reference
- 2500
- Primary DI / UDI-DI
- D06925000
- 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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