ClearanceBrief
510(k) K210132 ยท DZE Implant, Endosseous, Root-Form

s-Clean SQ-SL Implant System Regular

ApplicantDentis Co., Ltd., Daegu, KR
DecisionSubstantially Equivalent, Feb 17, 2021
ReceivedJan 19, 2021
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K210132

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.