ClearanceBrief
510(k) K233808 ยท DZE Implant, Endosseous, Root-Form

LW Narrow Implant System

ApplicantOssvis Co., Ltd., Anyang-Si, KR
DecisionSubstantially Equivalent, Jul 31, 2024
ReceivedNov 30, 2023
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K233808

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.