ClearanceBrief
510(k) K150344 ยท DZE Implant, Endosseous, Root-Form

Dentis Dental Implant System

ApplicantDentis Co., Ltd., Daegu, KR
DecisionSubstantially Equivalent, Jul 24, 2015
ReceivedFeb 11, 2015
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K150344

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.