ClearanceBrief
510(k) K253845 ยท LRK Device, Anti-Snoring

Anti Snoring Mouthpiece (L08-BP, L08-PT, L08-BT, L08-TP, L08-TB, L08-PB)

ApplicantRam.Shaw Pte. , Ltd., Singapore, SG
DecisionSubstantially Equivalent, Mar 3, 2026
ReceivedDec 2, 2025
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K253845

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.