K261251
- 510(k) number
- K261251
- Device name
- Snorbliss® Anti-Snoring Device
- Applicant
- Endeavor Commerce, LLC WY · US
- Product code
- LRK — Device, Anti-Snoring
- Decision date
- 2026-06-11
- Date received
- 2026-04-16
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Dental
PDFDownload 510(k) SummaryArchived here · 0.5 MB · U.S. public domain
Also available from FDA: K261251.pdf
Official FDA record: K261251
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.