# Eyekon Medical, Inc.

- Location (FDA's records): Clearwater
- FDA decisions: 2 (1989–2026): 1 510(k) clearance and 1 original PMA approval
- Product codes: HQL (1), MLP (1)
- Predicates its devices cite: 1 (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

## Firms whose devices it cites most
- Ocular Instruments, Inc.: 1 (https://510kreport.com/company/ocular-instruments)

## Recent decisions
- K261312: Temporary Keratoprosthesis (QuickSet TKP™) (Jul 24, 2026)
- P880072: Model P11 Modified J Loop Posterior Chamber Iol (Sep 22, 1989)

Source page: https://510kreport.com/company/eyekon-medical