Myosa (S1H, S1, S2, S3, S1M, S2M); Myosa for Snorers (S1, S1M, S2)
K-Number: K252531 · 2026-03-02
ApplicantMyofunctional Research Co.
Decision Date2026-03-02
Product CodeLRK
Advisory CommitteeDE
DecisionSubstantially Equivalent
Device Summary
Myosa (S1H, S1, S2, S3, S1M, S2M); Myosa for Snorers (S1, S1M, S2) is a medical device manufactured by Myofunctional Research Co.. It received FDA 510(k) clearance on 2026-03-02 under approval number K252531. The device is classified under product code LRK. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Myosa (S1H, S1, S2, S3, S1M, S2M); Myosa for Snorers (S1, S1M, S2)?
Myosa (S1H, S1, S2, S3, S1M, S2M); Myosa for Snorers (S1, S1M, S2) is a medical device that received FDA 510(k) clearance on 2026-03-02. It is manufactured by Myofunctional Research Co.. The 510(k) number is K252531.
When was Myosa (S1H, S1, S2, S3, S1M, S2M); Myosa for Snorers (S1, S1M, S2) approved by the FDA?
Myosa (S1H, S1, S2, S3, S1M, S2M); Myosa for Snorers (S1, S1M, S2) received FDA 510(k) clearance on 2026-03-02, under approval number K252531.
What company makes Myosa (S1H, S1, S2, S3, S1M, S2M); Myosa for Snorers (S1, S1M, S2)?
Myosa (S1H, S1, S2, S3, S1M, S2M); Myosa for Snorers (S1, S1M, S2) is manufactured by Myofunctional Research Co..
What is the FDA product code for Myosa (S1H, S1, S2, S3, S1M, S2M); Myosa for Snorers (S1, S1M, S2)?
The FDA product code for Myosa (S1H, S1, S2, S3, S1M, S2M); Myosa for Snorers (S1, S1M, S2) is LRK.
Related Devices (Code: LRK)
Official Source
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