3M™ 9667l
3M™ 9667l is a Class I device made by 3M Company, listed in FDA GUDID since 24 Sep 2018 (UDI-DI 00707387772215), 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 | Number00707387772215 | Date24 Sep 2018 | StatusListed |
Official records
- AccessGUDID record 00707387772215
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- 3M™
- Generic name
- Surgical hair clippers
- Model / Ref / Catalog
- 9667L
- Primary DI / UDI-DI
- 00707387772215
- FDA product code
- LWK
- GMDN term
- Surgical hair clippers
- Device class
- Class I
- Regulation number
- 878.4800
- GUDID distribution status
- In Commercial Distribution
Similar devices
Other devices filed under FDA product code LWK (RAZOR, SURGICAL).
- SURGICAL PREP RAZOR by Derma-Safe Co.
- Solventum™ 9667L-E by Solventum US LLC
- SensiClip 4403A by CAREFUSION 2200, INC.
- SURGICAL CLIPPER by Baxter Healthcare Corp
- Solventum™ 9661L by Solventum US LLC
- SURGICAL PREP RAZOR, STRAIGHT TYPE by Derma-Safe Co.
- 4406 by CAREFUSION 2200, INC.
- 3M(TM) SURGICAL SLIPPER, 9660 SERIES by WAHL CLIPPER CORP.