NWF
1 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Drill, Battery Powered, Subungual Hematoma
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 878.4820
- Medical specialty
- General, Plastic Surgery
- FDA definition
- Intended to cut a hole in finger and toe nails to release fluid accumulated in the underlying nail bed. Indicated to relieve pressure from subungual hematomas (including black toe).
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| PATHFORMER (K052770) | Path Scientific, LLC | 2005-10-31 |
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Every clearance here is in the API, with alerts when new ones post.