ClearanceBrief
510(k) K140934 ยท DZE Implant, Endosseous, Root-Form

HIOSSEN IMPLANT SYSTEM

ApplicantHiossen, Inc., Fariless Hills PA, US
DecisionSubstantially Equivalent, Nov 12, 2014
ReceivedApr 11, 2014
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K140934

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.