510(k) Report

FDA applicant

The Minnesota Back Brace Co.

Mchenry, IL1 decision1977–19770 recalls

FDA records 1 decision for The Minnesota Back Brace Co. (Mchenry, IL) in 1977: 1 510(k) clearance. All are in product code FHF (System, Evacuator, Fluid). 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, gastroenterology and urology panel, where it files most

How often FDA has decided The Minnesota Back Brace Co.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for The Minnesota Back Brace Co. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — The Minnesota Back Brace Co. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “The”

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