ClearanceBrief
510(k) K926354 ยท DZE Implant, Endosseous, Root-Form

ENDO-PORE ENDOSSEOUS DENTAL IMPLANT SYSTEM

ApplicantInnova Corp., Washington DC, US
DecisionSubstantially Equivalent, Feb 13, 1995
ReceivedDec 21, 1992
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K926354

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.