ClearanceBrief
510(k) K223924 ยท DZE Implant, Endosseous, Root-Form

LW Implant System

ApplicantOssvis Co., Ltd., Anyang-Si, KR
DecisionSubstantially Equivalent, Aug 8, 2023
ReceivedDec 30, 2022
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K223924

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.