FDA applicant

Humane Restraint, Inc.

Waunakee, WI1 decision1996–19960 recalls

FDA records 1 decision for Humane Restraint, Inc. (Waunakee, WI) in 1996: 1 510(k) clearance. All are in product code FMQ (Restraint, Protective). 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 Humane Restraint, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Humane Restraint, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Humane Restraint, Inc.

Which product codes does it file in?

What has FDA decided for it lately?