ClearanceBrief
510(k) K231097 · NHA Abutment, Implant, Dental, Endosseous

Inclusive® Titanium Abutments compatible with: Neoss® ProActive® Narrow, Neoss® ProActive® Standard, MIS® SEVEN®, Zimmer® Eztetic® Implant Systems

ApplicantPrismatik Dentalcraft, Inc., Irvine CA, US
DecisionSubstantially Equivalent, Nov 14, 2023
ReceivedApr 18, 2023
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K231097

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.