FDA applicant

American White Cross, Inc.

Stamford, CT10 decisions1985–19970 recalls

FDA records 10 decisions for American White Cross, Inc. (Stamford, CT) from 1985 to 1997: 10 510(k) clearances. Most are in product codes KGX (Tape And Bandage, Adhesive) and KMF (Bandage, Liquid). 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 hospital panel, where it files most

How often FDA has decided American White Cross, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for American White Cross, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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American White Cross, Inc.

Which product codes does it file in?

What has FDA decided for it lately?