Snorbliss® Anti-Snoring Device
K-Number: K261251 · 2026-06-11
Device Summary
Frequently Asked Questions
What is the Snorbliss® Anti-Snoring Device?
Snorbliss® Anti-Snoring Device is a medical device that received FDA 510(k) clearance on 2026-06-11. The listed applicant is Endeavor Commerce, LLC. The 510(k) number is K261251.
When did Snorbliss® Anti-Snoring Device receive FDA 510(k) clearance?
Snorbliss® Anti-Snoring Device received FDA 510(k) clearance on 2026-06-11, under 510(k) number K261251.
Who is the listed applicant for Snorbliss® Anti-Snoring Device?
The FDA 510(k) record lists Endeavor Commerce, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Snorbliss® Anti-Snoring Device?
The FDA product code for Snorbliss® Anti-Snoring Device is LRK.
Related Devices (Code: LRK)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.