FDA applicant

Eurotan Intl.

Houston, TX4 decisions1982–19860 recalls

FDA records 4 decisions for Eurotan Intl. (Houston, TX) from 1982 to 1986: 4 510(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 Eurotan Intl.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Eurotan Intl. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Eurotan Intl.

Which product codes does it file in?

What has FDA decided for it lately?