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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Device, Anti-Snoring
510(k) Number K261251
Device Name Snorbliss® Anti-Snoring Device
Applicant
Endeavor Commerce, LLC
30 N Gould St. Suite 47051
Sheridan,  WY  82801
Applicant Contact Hasem Basaran
Correspondent
Shanghai Spica Management Consulting Co., Ltd.
609 Rm., #133 Shengang Ave., Pudong New District
Shanghai,  CN 201306
Correspondent Contact Purity Chen
Regulation Number872.5570
Classification Product Code
LRK  
Date Received04/16/2026
Decision Date 06/11/2026
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Dental
510k Review Panel Dental
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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