LWK
4 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Razor, Surgical
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 878.4800
- Medical specialty
- General, Plastic Surgery
- Adverse events (MAUDE)
- 2013: 9 · 2014: 9 · 2016: 10 · 2017: 12 · 2019: 31 · 2026: 27
Reports received by FDA, not confirmed device causation - volume tracks device popularity as much as risk.
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| 3M(TM) SURGICAL SLIPPER, 9660 SERIES (K946162) | Wahl Clipper Corp. | 1995-01-24 |
| SURGICAL CLIPPER (K910524) | Baxter Healthcare Corp | 1991-03-28 |
| SURGICAL PREP RAZOR (K874370) | Derma-Safe Co. | 1987-11-13 |
| SURGICAL PREP RAZOR, STRAIGHT TYPE (K874234) | Derma-Safe Co. | 1987-11-02 |
Track LWK automatically
Every clearance here is in the API, with alerts when new ones post.