FDA applicant
The Minnesota Back Brace Co.
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
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.
Planning a device like The Minnesota Back Brace Co.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.
See the 510(k) ReportOther applicant names beginning “The”
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