ClearanceBrief
510(k) K250872 ยท DZE Implant, Endosseous, Root-Form

Bioline Dental Implant System

ApplicantBioline Dental Implant Systems, Ltd., Migdal Tefen, IL
DecisionSubstantially Equivalent, Jun 18, 2025
ReceivedMar 24, 2025
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K250872

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.