Medical Device Manufacturer · US , Mahwah , NJ

Seiko Corp. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1988

2

Total

2

Cleared

0

Denied

FDA 510(k) Regulatory Record - Seiko Corp. Ophthalmic ✕

2 devices

1-2 of 2

Cleared Jun 20, 1990

SPECTACLE FRAME

Ophthalmic · 124d

Cleared Nov 15, 1988

SEIKO P-6 PROGRESSIVE SPECTACLE LENSES

Ophthalmic · 29d

Data Source

Sourced from the FDA 510(k) public files . 175,972 total devices indexed.

Last updated: Apr 28, 2026