ClearanceBrief
510(k) K233865 ยท EKX Handpiece, Direct Drive, Ac-Powered

X-Smart Pro; X-Smart Pro+

ApplicantDentsply Sirona, Inc., York PA, US
DecisionSubstantially Equivalent, Jul 24, 2024
ReceivedDec 6, 2023
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K233865

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.