Hearing Innovations, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Model Wmr Bte Hearing Instrument (Model Wmr) Ref K963745
Regimes: 510(k) Registry: 510(k)Hisonic-Trd Tinnitus Relief Device Ref K013253
Regimes: 510(k) Registry: 510(k)Hi Sonic 2000 Digital Hearing Instrument Ref K951678
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Hearing Innovations, Inc. have in the registry?
The registry currently lists 3 devices for Hearing Innovations, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Hearing Innovations, Inc.'s devices?
Among its 3 most recently registered devices, Hearing Innovations, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Hearing Innovations, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Hearing Innovations, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Hearing Innovations, Inc. in the registry?
The most recently registered devices listed for Hearing Innovations, Inc. include MODEL WMR BTE HEARING INSTRUMENT (MODEL WMR), HISONIC-TRD TINNITUS RELIEF DEVICE and HI SONIC 2000 DIGITAL HEARING INSTRUMENT.