NBH
2 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Accessories, Arthroscopic
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 888.1100
- Medical specialty
- Orthopedic
- Adverse events (MAUDE)
- 2021: 389 · 2022: 334 · 2023: 492 · 2024: 676 · 2025: 561 · 2026: 329
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 |
|---|---|---|
| IRRIGATION SET (K822560) | Utah Medical Products, Inc. | 1982-12-03 |
| SHOVEL RETRACTOR (K822109) | Bio-Blitz, Inc. | 1982-07-30 |
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Every clearance here is in the API, with alerts when new ones post.