ClearanceBrief
510(k) K171795 ยท DZE Implant, Endosseous, Root-Form

Thommen Implant System

ApplicantThommen Medical AG, Grenchen, CH
DecisionSubstantially Equivalent, Sep 29, 2017
ReceivedJun 16, 2017
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K171795

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.