ClearanceBrief
510(k) K760768 ยท EKO Denture Preformed (Partially Prefabricated Denture)

FLEXIDENT DENTURE

ApplicantFlexodent Corp., Mchenry IL, US
DecisionSubstantially Equivalent, Oct 15, 1976
ReceivedOct 4, 1976
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K760768

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.