ClearanceBrief
510(k) K252187 ยท NFO Stimulator, Transcutaneous Electrical, Aesthetic Purposes

Aura Glide (FC40)

ApplicantAura Medical, LLC, Brooklyn NY, US
DecisionSubstantially Equivalent, Dec 23, 2025
ReceivedJul 14, 2025
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K252187

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.