# Chiron Intraoptics

- Location (FDA's records): Irvine, CA
- FDA decisions: 4 (1992–1993): 4 510(k) clearances
- Product codes: LYX (3), HQC (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 9 (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
- Al.Chi.Mi.A. S.R.L: 2 (https://510kreport.com/company/al-chi-mi-a)
- Alcon Laboratories: 2 (https://510kreport.com/company/alcon-laboratories)
- Numedis, Inc.: 1 (https://510kreport.com/company/numedis)
- Aurolab: 1 (https://510kreport.com/company/aurolab)
- Chiron Vision Corp.: 1 (https://510kreport.com/company/chiron-vision)
- Bausch & Lomb, Inc.: 1 (https://510kreport.com/company/bausch-lomb)
- Eurobio: 1 (https://510kreport.com/company/eurobio)

## Its most-cited devices
- K924165: Optisol-GS Corneal Storage Media (1992), cited by 5
- K925631: Phacotron Gold Multifunction Ultrasonic Handpiece (1993), cited by 3
- K921729: Optisol Corneal Storage Media Container/Modified (1992), cited by 1

## Recent decisions
- K925631: Phacotron Gold Multifunction Ultrasonic Handpiece (Jul 29, 1993)
- K924165: Optisol-GS Corneal Storage Media (Oct 6, 1992)
- K921728: Dexsol Corneal Storage Media Container, Modified (Jun 9, 1992)
- K921729: Optisol Corneal Storage Media Container/Modified (Jun 9, 1992)

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