FDA 510(k)

SnØreNegatØr

K-Number: K261912 · 2026-07-31

Decision Date2026-07-31

Product CodeLRK

Advisory CommitteeDE

DecisionSubstantially Equivalent

Device Summary

SnØreNegatØr is the device name listed in this FDA 510(k) record. The listed applicant is DnB Innovations, LLC. It received FDA 510(k) clearance on 2026-07-31 under 510(k) number K261912. 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 SnØreNegatØr?

SnØreNegatØr is a medical device that received FDA 510(k) clearance on 2026-07-31. The listed applicant is DnB Innovations, LLC. The 510(k) number is K261912.

When did SnØreNegatØr receive FDA 510(k) clearance?

SnØreNegatØr received FDA 510(k) clearance on 2026-07-31, under 510(k) number K261912.

Who is the listed applicant for SnØreNegatØr?

The FDA 510(k) record lists DnB Innovations, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SnØreNegatØr?

The FDA product code for SnØreNegatØr 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.

K261366VirtusSomnomed, Inc.K261251Snorbliss® Anti-Snoring DeviceEndeavor Commerce, LLC K261134Dormiva Anti-Snoring Mouth GuardKoncept Innovators, Inc.K252942ShaeferHShaeferh, LLC K253845Anti Snoring Mouthpiece (L08-BP, L08-PT, L08-BT, L08-TP, L08-TB, L08-PB)Ram.Shaw Pte. , Ltd.K252531Myosa (S1H, S1, S2, S3, S1M, S2M); Myosa for Snorers (S1, S1M, S2)Myofunctional Research Co.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.