510(k) Report

FDA applicant

Hamilton Industries, Inc.

Walker, MI5 decisions1977–19880 recalls

FDA records 5 decisions for Hamilton Industries, Inc. (Walker, MI) from 1977 to 1988: 5 510(k) clearances. Most are in product codes LGX (Table, Examination, Medical, Powered) and JOW (Sleeve, Limb, Compressible). 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 and plastic surgery panel, where it files most

How often FDA has decided Hamilton Industries, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Hamilton Industries, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Hamilton Industries, Inc.’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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Other applicant names beginning “Hamilton”

FDA records each applicant name separately; these may or may not be the same firm.