EJY
2 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Pliers, Operative
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 872.4565
- Medical specialty
- Dental
- 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 |
|---|---|---|
| 2710 TO 2935 VARIOUS PLIERS FOR ORTHODONTICS/PROST (K851730) | Artiberia | 1985-07-02 |
| BEACH SURGICAL PLIERS NON-HOOK (K821787) | Pacific Dental Corp. | 1982-07-06 |
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Every clearance here is in the API, with alerts when new ones post.