510(k) Report

FDA applicant

E.F. Brewer Co.

Menomonee Falls, WI4 decisions1982–19880 recalls

FDA records 4 decisions for E.F. Brewer Co. (Menomonee Falls, WI) from 1982 to 1988: 4 510(k) clearances. Most are in product codes FOX (Stand, Infusion) and KLC (Chair, Dental, With Operative Unit). 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 E.F. Brewer Co.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for E.F. Brewer Co. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like E.F. Brewer Co.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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