ClearanceBrief
510(k) K230203 ยท NHA Abutment, Implant, Dental, Endosseous

Dentis I-FIX Abutment

ApplicantDentis Co., Ltd., Daegu, KR
DecisionSubstantially Equivalent, May 3, 2023
ReceivedJan 25, 2023
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K230203

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.