Snorbliss® Anti-Snoring Device

FDA 510(k) K261251 · Endeavor Commerce, LLC

Substantially Equivalent

510(k) numberK261251

Submission

Device name
Snorbliss® Anti-Snoring Device
Applicant
Endeavor Commerce, LLC
Sheridan, WY, US
Received
April 16, 2026
Decision date
June 11, 2026
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
LRK – Device, Anti-Snoring
Device class
Class II (moderate risk)
Regulation
21 CFR 872.5570
Specialty
Dental

Other 510(k)s with product code LRK

510(k)DeviceApplicantDecision
K262104Anti Snoring Mouthpiece (L09-BB, L09-PP, L09-TB, L09-BT, L09-TP, L09-PT, L09-TT)LRK · Special Ram.Shaw Pte., Ltd.08/27/2026SE
K261912SnØreNegatØrLRK · Traditional DnB Innovations, LLC07/31/2026SE
K261366VirtusLRK · Special Somnomed, Inc.06/12/2026SE
K261134Dormiva Anti-Snoring Mouth GuardLRK · Special Koncept Innovators, Inc.05/14/2026SE
K252942ShaeferHLRK · Traditional Shaeferh, LLC04/10/2026SE
K253845Anti Snoring Mouthpiece (L08-BP, L08-PT, L08-BT, L08-TP, L08-TB, L08-PB)LRK · Traditional Ram.Shaw Pte. , Ltd.03/03/2026SE
K252531Myosa (S1H, S1, S2, S3, S1M, S2M); Myosa for Snorers (S1, S1M, S2)LRK · Traditional Myofunctional Research Co.03/02/2026SE
K252976Park Dental Nylon MADLRK · Traditional Park Dental Research Corp.12/18/2025SE
K253868QuietLab ProLRK · Traditional QuietLab, LLC12/05/2025SE
K252161Hushd AveraLRK · Abbreviated Good Sleep CO Pte , Ltd.11/25/2025SE

Questions and answers

When was Snorbliss® Anti-Snoring Device cleared by the FDA?

Snorbliss® Anti-Snoring Device (K261251) received a 510(k) decision of Substantially Equivalent on June 11, 2026, 56 days after the submission was received.

What is the product code of K261251?

The FDA product code is LRK – Device, Anti-Snoring, a Class II (moderate risk) device regulated under 21 CFR 872.5570.