# Menicon U.S.A., Inc.

- Location (FDA's records): Washington, DC
- FDA decisions: 3 (1997–2000): 3 510(k) clearances
- Product codes: HQD (2), LPL (1)
- Predicates its devices cite: 0 (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 that cite its devices most
- Menicon Co, Ltd.: 1 (https://510kreport.com/company/menicon)

## Its most-cited devices
- K970019: Menicon Z Bifocal Design Lens/Menicon Z Trifocal Design Lens (1997), cited by 1

## Recent decisions
- K000133: Menicon Z (May 19, 2000)
- K972443: Menicon SF-P and Menicon Z Rigid Gas Permeable Contact Lens (Aug 22, 1997)
- K970019: Menicon Z Bifocal Design Lens/Menicon Z Trifocal Design Lens (Mar 25, 1997)

Source page: https://510kreport.com/company/menicon-usa