K252531

Myosa (S1H, S1, S2, S3, S1M, S2M); Myosa for Snorers (S1, S1M, S2)

510(k) number: K252531
Device name: Myosa (S1H, S1, S2, S3, S1M, S2M); Myosa for Snorers (S1, S1M, S2)
Applicant: Myofunctional Research Co. AU
Product code: LRK — Device, Anti-Snoring
Decision date: 2026-03-02
Date received: 2025-08-12
Decision: Substantially Equivalent
Clearance type: Traditional
Advisory committee: Dental

Also available from FDA: K252531.pdf

Official FDA record: K252531

Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.