HLL
4 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Monitor, Eye Movement
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 886.1510
- Medical specialty
- Ophthalmic
- Flags
- Third-party review eligible
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| Retitrack (K222484) | C. Light Technologies, Inc. | 2023-05-09 |
| SACCADOMETER PLUS, SACCADOMETER ADVANCED (K152890) | Ober Consulting Sp. Z.O.O. | 2016-08-11 |
| VARILUX VISIONPRINT SYSTEM (VPS) (K033949) | Essilor Intl. | 2004-07-02 |
| ORTHOTONE (K872111) | Orthotone Corp. | 1988-11-16 |
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Every clearance here is in the API, with alerts when new ones post.