510(k) K252531

Device
Myosa (S1H, S1, S2, S3, S1M, S2M); Myosa for Snorers (S1, S1M, S2)
Applicant
Myofunctional Research Co.
510(k) number
K252531
Product code
LRK
Decision
Substantially Equivalent (SESE)
Decision date
2026-03-02
Date received
2025-08-12
Regulation
872.5570
Classification name
Device, Anti-Snoring
Medical specialty
Dental
Review panel
Dental
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
N

Related Records

Applicant Contact

Contact
Vikas Kundu
Address
44 Signato Dr. Helnsvale AU 4212 4212

FDA Registration Numbers

Source Documents

510(k) summary PDF

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