ClearanceBrief
510(k) K250504 ยท GEX Powered Laser Surgical Instrument

Leonardo Duster

ApplicantCeramoptec GmbH, Bonn, DE
DecisionSubstantially Equivalent, Jul 14, 2025
ReceivedFeb 20, 2025
TypeAbbreviated
FDA recordOpen on fda.gov

Recalls that name K250504

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.