ClearanceBrief
510(k) K192688 ยท DZE Implant, Endosseous, Root-Form

s-Clean SQ-SL Implant System Regular

ApplicantDentis Co., Ltd., Daegu, KR
DecisionSubstantially Equivalent, Feb 4, 2020
ReceivedSep 26, 2019
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K192688

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.