Snorbliss® Anti-Snoring Device— 510(k) K261251
Substantially EquivalentEndeavor Commerce, LLC
FDA 510(k) clearance K261251 for Snorbliss® Anti-Snoring Device, Substantially Equivalent on 2026-06-11. Applicant: Endeavor Commerce, LLC. Device class: 2.
Summary
Endeavor Commerce's Snorbliss Anti-Snoring Device is filed under LRK, anti-snoring devices. The record gives no model numbers or description beyond the name.
Class II, 21 CFR 872.5570. Dental is both the classification panel and the review panel. It came in as a Traditional 510(k).
Endeavor Commerce filed from Sheridan, Wyoming. The decision came 56 calendar days after FDA received it (April 16 to June 11, 2026).
Clearance details
- Applicant
- Endeavor Commerce, LLC
- Product code
- Product code LRK
- Device class
- Class 2
- Regulation
- 21 CFR 872.5570
- Advisory panel
- Dental
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Sheridan, WY, US
Recent devices under product code LRK
view allAdverse events under product code LRK
product code LRK- Injury
- 246
- Malfunction
- 1,044
- Total
- 1,290
Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →
Data sourced from openFDA. This site is unofficial and independent of the FDA.