510(k) K223694

Device
Tinearity G1 (6103); Tinearity G1 Adapters x3 (6042)
Applicant
Duearity AB
510(k) number
K223694
Product code
KLW
Decision
Substantially Equivalent (SESE)
Decision date
2023-06-30
Date received
2022-12-09
Regulation
874.3400
Classification name
Masker, Tinnitus
Medical specialty
Ear, Nose, Throat
Review panel
Ear, Nose, Throat
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
No

Related Records

Applicant Contact

Contact
Anneli Johansson
Address
Krusegrand 42d Malmo SE 21225 21225

FDA Registration Numbers

Source Documents

510(k) summary PDF

Related GUDID Devices

Primary DIBrandCompanyPublished
07350136210075TinearityDuearity AB2023-07-28
07350136210051Tinearity AdaptersDuearity AB2023-07-28

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K221125SilentCloudAureliym GmbH2023-01-04
K201370Multiflex Tinnitus TechnologyStarkey Laboratories, Inc.2020-06-19
K193303Tinnitus Sound Generator ModuleGN Hearing A/S2020-02-20
K180495Tinnitus Sound Generator ModuleGN Hearing A/S2018-11-30
K181586Tinnitus Sound Generator ModuleGN Hearing A/S2018-07-13
K171243audifon Tinnitus-ModuleAudiofon USA, Inc.2017-10-19
K163094TinniLogic Mobile Tinnitus Management DeviceJiangsu Betterlife Medical Co., Ltd.2017-05-17
K161562Sound Options Tinnitus TreatmentSound Options Tinnitus Treatments, Inc.2016-09-28
K161331HyperSound Tinnitus ModuleTurtle Beach Corporation2016-08-23
K151558Desyncra for Tinnitus Therapy System, Desyncra for Tinnitus Pro SystemNeurotherapies Reset GmbH2016-01-20
K151719REVE134Kw Ear Lab, Inc.2015-10-09
K150014SerenitySanuthera, Inc.2015-07-27
K150171Tinnitus Sound Generator ModuleGn Resound A/S2015-05-14