MQZ
4 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Prosthesis, Nail
- Device class
- Unclassified
- Medical specialty
- Unknown
- Adverse events (MAUDE)
- 1997: 2
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 |
|---|---|---|
| NailLift (K230841) | Jps Corporation | 2024-01-22 |
| Oniko nail brace (K162525) | Begum Saglik Hizmetleri Tibbi Malzemeler Danismanlik Lsti | 2018-04-25 |
| STOP-N-GROW (K960843) | European Touch Co., Inc. | 1996-08-12 |
| NAIL SPLINT (K850803) | Inro Medical Designs, Inc. | 1985-10-16 |
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Every clearance here is in the API, with alerts when new ones post.