# Midwest Ophthalmic Instruments, Inc.

- Location (FDA's records): Romeoville, IL
- FDA decisions: 1 (1995–1995): 1 510(k) clearance
- Product codes: HKI (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 2 (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
- Mrp Group, Inc.: 1 (https://510kreport.com/company/mrp-group)
- Tomey Corporation USA: 1 (https://510kreport.com/company/tomey-usa)

## Its most-cited devices
- K952480: Orims Digital Angiography System (1995), cited by 2

## Recent decisions
- K952480: Orims Digital Angiography System (Aug 25, 1995)

Source page: https://510kreport.com/company/midwest-ophthalmic-instruments