FDA applicant
Hamilton Kent
FDA records 1 decision for Hamilton Kent (Mchenry, IL) in 1981: 1 510(k) clearance. All are in product code KNP (Orthosis, Corrective Shoe). 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 Hamilton Kent’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Hamilton Kent since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Hamilton Kent’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 “Hamilton”
FDA records each applicant name separately; these may or may not be the same firm.