510(k) K251784

Device
Hushd Pro Z-Link
Applicant
Good Sleep CO Pte , Ltd.
510(k) number
K251784
Product code
LRK
Decision
Substantially Equivalent (SESE)
Decision date
2025-10-24
Date received
2025-06-11
Regulation
872.5570
Classification name
Device, Anti-Snoring
Medical specialty
Dental
Review panel
Dental
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
N

Related Records

Applicant Contact

Contact
Alwin Ngai
Address
105 Cecil St. #18-18, The Octagon Singapore SG 069534 069534

FDA Registration Numbers

Source Documents

510(k) summary PDF

Other 510(k) Records For Product Code LRK

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K261134Dormiva Anti-Snoring Mouth GuardKoncept Innovators, Inc.2026-05-14
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K253845Anti Snoring Mouthpiece (L08-BP, L08-PT, L08-BT, L08-TP, L08-TB, L08-PB)Ram.Shaw Pte. , Ltd.2026-03-03
K252531Myosa (S1H, S1, S2, S3, S1M, S2M); Myosa for Snorers (S1, S1M, S2)Myofunctional Research Co.2026-03-02
K252976Park Dental Nylon MADPark Dental Research Corp.2025-12-18
K253868QuietLab ProQuietLab, LLC2025-12-05
K252161Hushd AveraGood Sleep CO Pte , Ltd.2025-11-25
K252525AIO BreatheAiomega, LLC2025-11-06
K252698NightGuard Aire MaxNightguard Express, LLC2025-11-03
K253355Difiney Advanced Anti Snoring Device 4.0Fissiontech, LLC2025-10-29
K251628Mandibular Advancement Device L07Dcstar, Inc.2025-10-22
K250028Anti Snore MouthpieceDongguan Yiyao Science & Technology Development Co., Ltd.2025-10-03
K243752Double Tube Herbst ApplianceThe Tmj Clinic PC2025-09-17
K252374Nylon flexTAP(R)Airway Technologies D/B/A Airway Management2025-09-11
K250353Oniris; Oniris PlusOniris2025-09-04