Forefoot II 159225SND
by Newdeal Sas
Forefoot II 159225SND is a Class I device made by Newdeal Sas, listed in FDA GUDID since 16 Oct 2018 (UDI-DI 10381780055877), registry data as of 23 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 | Number10381780055877 | Date16 Oct 2018 | StatusListed |
Official records
- AccessGUDID record 10381780055877
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Forefoot II
- Generic name
- Fluted surgical drill bit, single-use
- Model / Ref / Catalog
- 159225SND
- Primary DI / UDI-DI
- 10381780055877
- FDA product code
- HTW
- GMDN term
- Fluted surgical drill bit, single-use
- Device class
- Class I
- Regulation number
- 888.4540
- GUDID distribution status
- In Commercial Distribution
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