FDA applicant

Mowbray Co., Inc.

Waterloo, IA1 decision1985–19850 recalls

FDA records 1 decision for Mowbray Co., Inc. (Waterloo, IA) in 1985: 1 510(k) clearance. All are in product code KGT (Drape, Adhesive, Aerosol). 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 Mowbray Co., Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Mowbray Co., Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Mowbray Co., Inc.

Which product codes does it file in?

What has FDA decided for it lately?