510(k) K202529

Device
ProSomnus EVO Sleep and Snore Device, ProSomnus EVO Sleep and Snore Device with Patient Monitoring
Applicant
Prosomnus Sleep Technologies, Inc.
510(k) number
K202529
Product code
LRK
Decision
Substantially Equivalent (SESE)
Decision date
2020-11-20
Date received
2020-09-01
Regulation
872.5570
Classification name
Device, Anti-Snoring
Medical specialty
Dental
Review panel
Dental
Device class
2
Clearance type
Special
Statement or summary
Summary
Third party reviewed
No

Applicant Contact#

Contact
Divya Mavalli
Address
5860 W. Las Positas Blvd. Pleasanton CA US 94588 94588

FDA Registration Numbers#

Source Documents#

510(k) summary PDF

Other 510(k) Records For Product Code LRK#

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K261134Dormiva Anti-Snoring Mouth GuardKoncept Innovators, Inc.2026-05-14
K252942ShaeferHShaeferh, LLC2026-04-10
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
K251784Hushd Pro Z-LinkGood Sleep CO Pte , Ltd.2025-10-24
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