ClearanceBrief
510(k) K170031 ยท DZE Implant, Endosseous, Root-Form

Internal Octa Implant System

ApplicantEbi, Inc., Gyeongsan-Si, KR
DecisionSubstantially Equivalent, Aug 31, 2017
ReceivedJan 4, 2017
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K170031

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.