FDA applicant

Nordic Sun Corporation of America

Stamford, CT2 decisions1986–19860 recalls

FDA records 2 decisions for Nordic Sun Corporation of America (Stamford, CT) in 1986: 2 510(k) clearances. All are in product code FTC (Light, Ultraviolet, Dermatological). 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, general and plastic surgery panel, where it files most

How often FDA has decided Nordic Sun Corporation of America’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Nordic Sun Corporation of America since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Nordic Sun Corporation of America 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 Eyewear, Inc. 1 Nordic Kinetics AB 1

Nordic Sun Corporation of America

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Nordic”