HNX
2 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Depressor, Orbital
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 886.4350
- Medical specialty
- Ophthalmic
- Adverse events (MAUDE)
- 2000: 1
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 |
|---|---|---|
| FMS HIGH FLOW ARTHRO-SHEATH (K951702) | Future Medical Systems, Inc. | 1995-05-12 |
| FMS ARTHRO-CUTTER (K951701) | Future Medical Systems, Inc. | 1995-05-09 |
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Every clearance here is in the API, with alerts when new ones post.