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FDA 510(k)

Snorbliss® Anti-Snoring Device

K-Number: K261251 · 2026-06-11

Decision Date2026-06-11
Product CodeLRK
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

Snorbliss® Anti-Snoring Device is the device name listed in this FDA 510(k) record. The listed applicant is Endeavor Commerce, LLC. It received FDA 510(k) clearance on 2026-06-11 under 510(k) number K261251. The device is classified under product code LRK. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

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

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