ClearanceBrief
510(k) K234049 · DZE Implant, Endosseous, Root-Form

Straumann® BLC and TLC Implants - Line extension

ApplicantInstitut Straumann AG, Basel, CH
DecisionSubstantially Equivalent, Mar 20, 2024
ReceivedDec 21, 2023
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K234049

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.