# Chiron Ophthalmics

- Location (FDA's records): Irvine, CA
- FDA decisions: 11 (1988–1992): 10 510(k) clearances and 1 original PMA approval
- Product codes: MOE (6), HQL (2), KYB (2), LYX (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 3 (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 that cite its devices most
- Alcon Laboratories: 2 (https://510kreport.com/company/alcon-laboratories)
- Chiron Vision Corp.: 1 (https://510kreport.com/company/chiron-vision)

## Its most-cited devices
- K903574: Chiroflex Lens Microsert (1990), cited by 2
- K914311: Chiroflex II Lens Microsert (TM) (1992), cited by 1

## Recent decisions
- K915861: Medilens-CS Corneal Shield (Mar 6, 1992)
- K914311: Chiroflex II Lens Microsert (TM) (Jan 27, 1992)
- K905825: Collagen Shield, Various Models (Jun 10, 1991)
- K903575: Chiroflex Forceps (Dec 21, 1990)
- K903574: Chiroflex Lens Microsert (Sep 17, 1990)
- K901880: Medilens (TM) Corneal Shield (Jul 2, 1990)
- K894162: Optisol (Jan 12, 1990)
- P890068: Model P-11 Modified J-Loop Posterior Chamber Iol (Jan 11, 1990)

Source page: https://510kreport.com/company/chiron-ophthalmics