# Seiko Optical Products of America, Inc.

- Location (FDA's records): Mahwah, NJ
- FDA decisions: 4 (1986–1994): 4 510(k) clearances
- Product codes: HQG (2), HQY (1), HQZ (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K942513: Seiko Eyeglass Frame (Jul 15, 1994)
- K900764: Sunglass, Non-Prescription (Jun 20, 1990)
- K873245: AR Diacoat Single Vision Lenses (Oct 5, 1987)
- K861684: Seiko P-2 & Seiko P-3 (Spectacle Lens) (Jun 9, 1986)

Source page: https://510kreport.com/company/seiko-optical-products-of-america