ClearanceBrief
510(k) K142313 ยท DZE Implant, Endosseous, Root-Form

OneQ-SL Implant System

ApplicantDentis Co., Ltd., Daegu, KR
DecisionSubstantially Equivalent, Dec 10, 2015
ReceivedAug 19, 2014
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K142313

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.