ClearanceBrief
510(k) K253468 · MPA Endoilluminator

Nova Eye iTrack™ 250A Canaloplasty Microcatheter (iTrack™ 250A)

ApplicantNova Eye, Inc., Fremont CA, US
DecisionSubstantially Equivalent, Aug 10, 2026
ReceivedOct 9, 2025
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K253468

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.