# Opko Instrumentation, Inc.

- Location (FDA's records): Miami, FL
- FDA decisions: 1 (2009–2009): 1 510(k) clearance
- Product codes: IYO (1)
- Predicates its devices cite: 3 (0 its own); citations of its devices by later devices: 1 (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
- Ophthalmic Technologies, Inc.: 3 (https://510kreport.com/company/ophthalmic-technologies)

## Firms that cite its devices most
- Accutome, Inc.: 1 (https://510kreport.com/company/accutome)

## Its most-cited devices
- K092837: Oti-Scan 3000 (2009), cited by 1

## Recent decisions
- K092837: Oti-Scan 3000 (Dec 23, 2009)

Source page: https://510kreport.com/company/opko-instrumentation