FDA applicant

Euro-Med Intl.

Danville, CA16 decisions1985–19880 recalls

FDA records 16 decisions for Euro-Med Intl. (Danville, CA) from 1985 to 1988: 16 510(k) clearances. Most are in product codes KDC (Instrument, Surgical, Disposable) and FZS (Curette, Surgical, General Use). 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 Euro-Med Intl.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Euro-Med Intl. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Euro-Med Intl.

Which product codes does it file in?

What has FDA decided for it lately?