ClearanceBrief
510(k) K252246 ยท JEY Plate, Bone

Leforte MMF System

ApplicantJeil Medical Corporation, Seoul, KR
DecisionSubstantially Equivalent, Apr 2, 2026
ReceivedJul 18, 2025
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K252246

No recall in the FDA data names this 510(k).

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.