ClearanceBrief
510(k) K262104 ยท LRK Device, Anti-Snoring

Anti Snoring Mouthpiece (L09-BB, L09-PP, L09-TB, L09-BT, L09-TP, L09-PT, L09-TT)

ApplicantRam.Shaw Pte., Ltd., Singapore, SG
DecisionSubstantially Equivalent, Aug 27, 2026
ReceivedJun 23, 2026
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K262104

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.