HLF
3 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Device, Measuring, Lens Radius, Ophthalmic
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 886.1430
- Medical specialty
- Ophthalmic
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| MARCO STANDARD RADIUSGAUGES (K930437) | Marco Ophthalmic, Inc. | 1993-08-09 |
| BAUSCH & LOMB CONTACT LENS VIEWER (K862517) | Bausch & Lomb, Inc. | 1986-08-11 |
| ERG-JET ELECTRODE (K823767) | Life-Tech Intl., Inc. | 1983-01-08 |
Track HLF automatically
Every clearance here is in the API, with alerts when new ones post.