ClearanceBrief
510(k) K231940 · NHA Abutment, Implant, Dental, Endosseous

BruxZir® NOW SRC

ApplicantPrismatik Dentalcraft, Inc., Irvine CA, US
DecisionSubstantially Equivalent, May 15, 2024
ReceivedJun 30, 2023
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K231940

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.