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FDA 510(k)

Anti Snore Mouthpiece

K-Number: K250028 · 2025-10-03

Decision Date2025-10-03
Product CodeLRK
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

Anti Snore Mouthpiece is a medical device manufactured by Dongguan Yiyao Science & Technology Development Co., Ltd.. It received FDA 510(k) clearance on 2025-10-03 under approval number K250028. 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 Anti Snore Mouthpiece?

Anti Snore Mouthpiece is a medical device that received FDA 510(k) clearance on 2025-10-03. It is manufactured by Dongguan Yiyao Science & Technology Development Co., Ltd.. The 510(k) number is K250028.

When was Anti Snore Mouthpiece approved by the FDA?

Anti Snore Mouthpiece received FDA 510(k) clearance on 2025-10-03, under approval number K250028.

What company makes Anti Snore Mouthpiece?

Anti Snore Mouthpiece is manufactured by Dongguan Yiyao Science & Technology Development Co., Ltd..

What is the FDA product code for Anti Snore Mouthpiece?

The FDA product code for Anti Snore Mouthpiece is LRK.

Related Devices (Code: LRK)

Official Source

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