FDA applicant

Arbrook Mfg. Corp.

Mchenry, IL5 decisions1976–19790 recalls

FDA records 5 decisions for Arbrook Mfg. Corp. (Mchenry, IL) from 1976 to 1979: 5 510(k) clearances. Most are in product codes KGO (Surgeon'S Gloves) and FMC (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 hospital panel, where it files most

How often FDA has decided Arbrook Mfg. Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Arbrook Mfg. Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Arbrook Mfg. Corp.

Which product codes does it file in?

What has FDA decided for it lately?