FDA applicant

Eureka Optics, Inc.

Toegu, Korea, KR1 decision1990–19900 recalls

FDA records 1 decision for Eureka Optics, Inc. (Toegu, Korea, KR) in 1990: 1 510(k) clearance. All are in product code HQZ (Frame, Spectacle). 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 Eureka Optics, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Eureka Optics, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Eureka”

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

Eureka X-Ray Tube Corp. 2 Eureka Laboratories, Inc. 1 Eureka AB 1

Eureka Optics, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Eureka”