510(k) K261251

Snorbliss® Anti-Snoring Device by Endeavor Commerce, LLC — Product Code LRK

K261251 is an FDA 510(k) premarket notification submitted by Endeavor Commerce, LLC for the device "Snorbliss® Anti-Snoring Device". The FDA issued a decision of Substantially Equivalent on June 11, 2026. The device falls under product code LRK (Device, Anti-Snoring), a Class II device regulated under 21 CFR 872.5570.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
June 11, 2026
Date Received
April 16, 2026
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Device, Anti-Snoring
Device Class
Class II
Regulation Number
872.5570
Review Panel
DE
Submission Type