# Carl Zeiss Ophthalmic Systems, Inc.

- Location (FDA's records): Dublin, CA
- FDA decisions: 2 (2002–2002): 2 510(k) clearances
- Product codes: IYO (1), NFF (1)
- Predicates its devices cite: 1 (0 its own); citations of its devices by later devices: 7 (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
- Carl Zeiss Jena GmbH: 1 (https://510kreport.com/company/carl-zeiss-jena)

## Firms that cite its devices most
- Carl Zeiss Meditec, AG: 2 (https://510kreport.com/company/carl-zeiss-meditec)
- Opto Global, Inc.: 1 (https://510kreport.com/company/opto-global)
- Heidelberg Engineering GmbH: 1 (https://510kreport.com/company/heidelberg-engineering)
- Bioptigen, Inc.: 1 (https://510kreport.com/company/bioptigen)
- Optovue, Inc.: 1 (https://510kreport.com/company/optovue)
- Medivision Medical Imaging, Ltd.: 1 (https://510kreport.com/company/medivision-medical-imaging)

## Its most-cited devices
- K012727: Humphrey OCT3 (2002), cited by 4
- K021787: Visucam (2002), cited by 3

## Recent decisions
- K021787: Visucam (Jun 21, 2002)
- K012727: Humphrey OCT3 (Jan 31, 2002)

Source page: https://510kreport.com/company/carl-zeiss-ophthalmic-systems