510(k) K093710

Device
THE MOSES APPLIANCE
Applicant
ALLEN J. MOSES, DDS, LTD.
510(k) number
K093710
Product code
LRK  
Decision
Substantially Equivalent (SESE)
Decision date
2010-05-12
Date received
2009-12-02
Regulation
872.5570
Classification name
Device, Anti-snoring
Medical specialty
Dental
Review panel
Dental
Device class
2
Clearance type
Abbreviated
Statement or summary
Statement
Third party reviewed
No

Applicant Contact#

Contact
ALLEN J MOSES
Address
233 S. Wacker Dr. Chicago IL US 60606 60606

FDA Registration Numbers#

Source Documents#

510(k) summary PDF not indicated by FDA

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

Legacy Summary#

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FDA Review#

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