FDA applicant

Seiko Corp.

Mahwah, NJ2 decisions1988–19900 recalls

FDA records 2 decisions for Seiko Corp. (Mahwah, NJ) from 1988 to 1990: 2 510(k) clearances. Most are in product codes HQZ (Frame, Spectacle) and HQG (Lens, Spectacle, Non-Custom (Prescription)). No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, ophthalmic panel, where it files most

How often FDA has decided Seiko Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Seiko Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Seiko Corp. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “Seiko”

FDA records each applicant name separately; these may or may not be the same firm.

Seiko Optical Products of America, Inc. 4 Seiko Instruments USA, Inc. 2

Seiko Corp.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Seiko”