FDA.reportPublic FDA data

510(k) K230532

Device
RADx Intraoral Appliance for Snoring and Sleep Apnea
Applicant
Achaemenid, LLC
510(k) number
K230532
Product code
LQZ
Decision
Substantially Equivalent (SESE)
Decision date
2023-07-12
Date received
2023-02-27
Regulation
872.5570
Classification name
Device, Jaw Repositioning
Medical specialty
Dental
Review panel
Dental
Device class
2
Clearance type
Abbreviated
Statement or summary
Summary
Third party reviewed
No

Applicant Contact#

Contact
Rachel Miller
Address
2318 Main St. Stratford CT US 06615 06615

FDA Registration Numbers#

Source Documents#

510(k) summary PDF

Other 510(k) Records For Product Code LQZ#

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K233754AIO BreatheAiomega, LLC2024-02-23
K203712The SlideBiotex, Inc.2021-07-20
K191320Slow Wave DS8Slow Wave, Inc.2020-10-02
K192581The NightBlocks ApplianceAdvanced Facialdontics, LLC2020-01-28
K162816SML-OSA2 AppliancesSelane Products, Inc.2017-07-27
K130130ATG/SM-OSA APPLIANCESSelane Products, Inc.2013-08-26
K112627MILLENIUM ANTI-SNORING DEVICEMillenium Dental Laboratory, Inc.2012-06-06
K112766SNORKELFellmar Company2012-06-04
K113201NARVAL CCResmed Sas2011-12-01
K090911IST SNORING APPLIANCEDental Crafters2009-09-11
K091035FULL BREATH SLEEP APPLIANCE LOWER (FBSL)Bryan Keropian Dds2009-06-24
K061228FULL BREATH SLEEP APPLIANCE WITH POSTERIOR TONGUE DEPRESSORBryan Keropian Dds2006-05-26
K053065FULL BREATH SLEEP APPLIANCE - PB (POSTERIOR BITE AND PBB (POSTERIOR BITE WITH BUMPS)Bryan Keropian Dds2006-01-03
K052862FULL BREATH SLEEP APPLIANCE - AB (ANTERIOR BITE)Bryan Keropian Dds2005-12-30
K032410SNORENTIJames P Boyd2005-02-28