FDA applicant

General Scientific Corp.

Ann Arbor, MI1 decision1994–19940 recalls

FDA records 1 decision for General Scientific Corp. (Ann Arbor, MI) in 1994: 1 510(k) clearance. All are in product code HOH (Spectacle, Operating (Loupe), Ophthalmic). 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 General Scientific Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for General Scientific Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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General Scientific Corp.

Which product codes does it file in?

What has FDA decided for it lately?