# Miami Eye Technology, Inc.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 6 (1983–1984): 6 510(k) clearances
- Product codes: HNY (1), HJO (1), HNH (1), HQC (1), HPN (1), HKY (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K841101: Clayman-Parel Capsule Coupeur (May 16, 1984)
- K832912: Gelender Vacuum Fixation Ring Sys (Jan 10, 1984)
- K832996: Surgical Iop Monitor (Nov 28, 1983)
- K832997: Epa Automated Infusion Pole (Oct 4, 1983)
- K832911: Abbott Globe Holder (Sep 29, 1983)
- K831702: Rare-Earth Intra-Ocular Magnet (Jun 30, 1983)

Source page: https://510kreport.com/company/miami-eye-technology