ClearanceBrief
510(k) K240383 ยท DZE Implant, Endosseous, Root-Form

Highness Implant System

ApplicantHighness Co., Ltd., Gyeongsangbuk-Do, KR
DecisionSubstantially Equivalent, Oct 31, 2024
ReceivedFeb 8, 2024
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K240383

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.