FDA applicant

Wall Manufacturer, Inc.

Walker, MI1 decision1982–19820 recalls

FDA records 1 decision for Wall Manufacturer, Inc. (Walker, MI) in 1982: 1 510(k) clearance. All are in product code ILM (Bath, Sitz, Powered). 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 Wall Manufacturer, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Wall Manufacturer, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Wall Manufacturer, Inc.

Which product codes does it file in?

What has FDA decided for it lately?