ClearanceBrief
510(k) K083586 ยท DZE Implant, Endosseous, Root-Form

I-FIX SYSTEM

ApplicantDentis Co., Ltd., Santa Fe Springs CA, US
DecisionSubstantially Equivalent, Apr 29, 2009
ReceivedDec 4, 2008
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K083586

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.