ClearanceBrief
510(k) K251957 ยท SFD In Situ Polymerizing Peripheral Nerve Repair Device

Coaptium Connect with Tissium Light

ApplicantTissium SA, Paris, FR
DecisionSubstantially Equivalent, Sep 8, 2025
ReceivedJun 25, 2025
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K251957

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.