K261366
- 510(k) number
- K261366
- Device name
- Virtus
- Applicant
- Somnomed, Inc. TX · US
- Product code
- LRK — Device, Anti-Snoring
- Decision date
- 2026-06-12
- Date received
- 2026-04-27
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Dental
510(k) Summary (official FDA PDF): K261366.pdf
Official FDA record: K261366
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.