Henry Schein 9007665
by Henry Schein, Inc. 2 variants
Henry Schein 9007665 is a safety razor (FDA Class I; FDA product code LWK, Razor, Surgical) made by Henry Schein, Inc., listed in FDA GUDID since 31 Jan 2019 (UDI-DI H70490076651), 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 | NumberH70490076651 | Date31 Jan 2019 | StatusListed |
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Henry Schein
- Generic name
- Safety razor, single-use
- Model / Ref / Catalog
- 9007665
- Primary DI / UDI-DI
- H70490076651
- FDA product code
- LWK
- GMDN term
- Safety razor, single-use
- Device class
- Class I
- Regulation number
- 878.4800
- GUDID distribution status
- In Commercial Distribution
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Other devices filed under FDA product code LWK (RAZOR, SURGICAL).
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- 4412A by CAREFUSION 2200, INC.
- SURGICAL PREP RAZOR by Derma-Safe Co.
- Solventum™ 9667L-E by Solventum US LLC
- SURGICAL CLIPPER by Baxter Healthcare Corp
- SURGICAL PREP RAZOR, STRAIGHT TYPE by Derma-Safe Co.
- 3M(TM) SURGICAL SLIPPER, 9660 SERIES by WAHL CLIPPER CORP.