ClearanceBrief
510(k) K232049 ยท DZE Implant, Endosseous, Root-Form

IS-III active Short Implant

ApplicantNeobiotech Co., Ltd., Seoul, KR
DecisionSubstantially Equivalent, Mar 28, 2024
ReceivedJul 10, 2023
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K232049

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.