ClearanceBrief
510(k) K243336 · EBI Resin, Denture, Relining, Repairing, Rebasing

Lucitone Digital Print Denture™ System

ApplicantDentsply Sirona, Inc., York PA, US
DecisionSubstantially Equivalent, Dec 17, 2024
ReceivedOct 24, 2024
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K243336

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.