FDA applicant

Lowenkamp Intl., Inc.

Hazlehurst, MS4 decisions1990–19950 recalls

FDA records 4 decisions for Lowenkamp Intl., Inc. (Hazlehurst, MS) from 1990 to 1995: 4 510(k) clearances. Most are in product codes LYY (Latex Patient Examination Glove) and KGO (Surgeon'S Gloves). 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 Lowenkamp Intl., Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Lowenkamp Intl., Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Lowenkamp Intl., Inc.

Which product codes does it file in?

What has FDA decided for it lately?