ClearanceBrief
510(k) K932123 ยท DZE Implant, Endosseous, Root-Form

IMPLANT INNOVATION PRE-ANGLED ABUTMENT SYSTEM

ApplicantImplant Innovations International, Inc., West Palm Baeach FL, US
DecisionSubstantially Equivalent, May 27, 1994
ReceivedMay 3, 1993
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K932123

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.