HTF
3 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Curette
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 878.4800
- Medical specialty
- General, Plastic Surgery
- Adverse events (MAUDE)
- 2005: 2 · 2008: 3 · 2010: 5 · 2013: 10 · 2021: 16 · 2025: 20
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 |
|---|---|---|
| BONE CURETTE (K890252) | Kinetic Medical Products | 1989-01-27 |
| ACROMED WALLIE-HEINIG CURETTES (K870778) | Buckman Co., Inc. | 1987-03-09 |
| 4MM CUP CURRETTE (K841979) | Stainless Mfg., Inc. | 1984-06-19 |
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Every clearance here is in the API, with alerts when new ones post.