ClearanceBrief
510(k) K160213 ยท DZE Implant, Endosseous, Root-Form

s-Clean Tapered II RBM Implant System

ApplicantDentis Co., Ltd., Daegu, KR
DecisionSubstantially Equivalent, Jun 21, 2016
ReceivedJan 29, 2016
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K160213

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.