FDA applicant

Nordic Eyewear, Inc.

Mchenry, IL1 decision1982–19820 recalls

FDA records 1 decision for Nordic Eyewear, Inc. (Mchenry, IL) in 1982: 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 Nordic Eyewear, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Nordic Eyewear, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Nordic Eyewear, 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 “Nordic”

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

Nordic Sun Corporation of America 2 Nordic Kinetics AB 1

Nordic Eyewear, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Nordic”