FDA applicant

Manuco Manufacturing Co., Inc.

Mchenry, IL4 decisions1982–19820 recalls

FDA records 4 decisions for Manuco Manufacturing Co., Inc. (Mchenry, IL) in 1982: 4 510(k) clearances. Most are in product codes ITJ (Walker, Mechanical) and IPS (Cane). 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, physical medicine panel, where it files most

How often FDA has decided Manuco Manufacturing Co., Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Manuco Manufacturing Co., Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Manuco Manufacturing Co., Inc.

Which product codes does it file in?

What has FDA decided for it lately?