FDA applicant
Cintor Orthopaedic Div.
FDA records 7 decisions for Cintor Orthopaedic Div. (Mchenry, IL) from 1980 to 1981: 7 510(k) clearances. Most are in product codes JDI (Prosthesis, Hip, Semi-Constrained…) and HSB (Rod, Fixation, Intramedullary And Accessories). 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 Cintor Orthopaedic Div.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Cintor Orthopaedic Div. since 2007.
Recalls per year
No recall linked to its devices since 2007.
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