# Optonol, Ltd.

- Location (FDA's records): Rockville, MD
- FDA decisions: 2 (2002–2003): 2 510(k) clearances
- Product codes: KYF (2)
- Predicates its devices cite: 5 (1 its own); citations of its devices by later devices: 2 (1 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
- New World Medical, Inc.: 1 (https://510kreport.com/company/new-world-medical)
- Optimed, Inc.: 1 (https://510kreport.com/company/optimed)
- Wright Medical Corp.: 1 (https://510kreport.com/company/wright-medical)
- Pharmacia Iovision, Inc.: 1 (https://510kreport.com/company/pharmacia-iovision)

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

## Its most-cited devices
- K012852: EX-Press Minature Glaucoma Implant, Models R-20, R-30, R-50, STS Versions (2002), cited by 2

## Recent decisions
- K030350: Express Mini Glaucoma Shunt (Mar 13, 2003)
- K012852: EX-Press Minature Glaucoma Implant, Models R-20, R-30, R-50, STS Versions (Mar 26, 2002)

Source page: https://510kreport.com/company/optonol