FDA applicant

Podiatry Products Corp.

Walker, MI1 decision1982–19820 recalls

FDA records 1 decision for Podiatry Products Corp. (Walker, MI) in 1982: 1 510(k) clearance. All are in product code FQL (Stocking, Medical Support (For General Medical…). 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 Podiatry Products Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Podiatry Products Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Podiatry Products Corp.

Which product codes does it file in?

What has FDA decided for it lately?