ClearanceBrief
510(k) K251230 ยท GEX Powered Laser Surgical Instrument

The Alma Hybrid Laser System

ApplicantAlma Lasers, Inc., Buffalo Grove IL, US
DecisionSubstantially Equivalent, May 21, 2025
ReceivedApr 21, 2025
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K251230

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.