FDA applicant

American Pro Latex, Inc.

Glenview, IL5 decisions1990–19970 recalls

FDA records 5 decisions for American Pro Latex, Inc. (Glenview, IL) from 1990 to 1997: 5 510(k) clearances. Most are in product codes KGO (Surgeon'S Gloves) and LYY (Latex Patient Examination Glove). 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 American Pro Latex, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for American Pro Latex, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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American Pro Latex, Inc.

Which product codes does it file in?

What has FDA decided for it lately?