ClearanceBrief
510(k) K211052 ยท DZE Implant, Endosseous, Root-Form

Straumann RidgeFit Implants

ApplicantInstitut Straumann AG, Basel, CH
DecisionSubstantially Equivalent, Jul 8, 2021
ReceivedApr 9, 2021
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K211052

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.