HXG
1 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Tamp
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 888.4540
- Medical specialty
- Orthopedic
- Adverse events (MAUDE)
- 2007: 9 · 2008: 3 · 2009: 8 · 2010: 5 · 2019: 15 · 2025: 25
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 |
|---|---|---|
| PUNCH (K841626) | Plastafil, Inc. | 1984-08-27 |
Track HXG automatically
Every clearance here is in the API, with alerts when new ones post.