HOG
5 FDA 510(k) clearances · Product code
97 daysmedian time to decision
161 days90th percentile
5clearances measured
FDA profile
- Official device name
- Burr, Corneal, Battery-Powered
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 886.4070
- Medical specialty
- Ophthalmic
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| AMOILS EPITHELIAL SCRUBBER (K962989) | S. Percy Amoils | 1997-01-09 |
| PALLIKARIS BRUSH (K960261) | Alcon Laboratories, Inc. | 1996-03-11 |
| BURR, CORNEAL, BATTERY-POWERED (K950520) | Aaron Medical Industries | 1995-05-02 |
| GY-RO SAFE (K883785) | Gy-Ro Industry, Inc. | 1989-01-05 |
| OPHTEC RUST RING REMOVER (K834354) | Jedmed Instrument Co. | 1984-03-19 |
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Every clearance here is in the API, with alerts when new ones post.