Sonovation, Inc. Dba Avr Sonovation
United StatesFDA applicant, unverified
- Devices
- 2
What Sonovation, Inc. Dba Avr Sonovation makes
Sonovation, Inc. manufactures the EXTEND-EAR, a device designed for ear canal expansion, and the Model FT40 Transonic™ hearing aid, a hearing assistance device.
These products are classified as Class I medical devices and are listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Extend-Ear Ref K920466
Regimes: 510(k) Registry: 510(k)Model FT40 Transonic(Tm) Hearing Aid Ref K905516
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Sonovation, Inc. Dba Avr Sonovation have in the registry?
The registry currently lists 2 devices for Sonovation, Inc. Dba Avr Sonovation. Devices recorded under merged duplicate company entries are counted once.
Which registries list Sonovation, Inc. Dba Avr Sonovation's devices?
Among its 2 most recently registered devices, Sonovation, Inc. Dba Avr Sonovation has devices listed in FDA 510(k) (2 devices).
What risk classes do Sonovation, Inc. Dba Avr Sonovation's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Sonovation, Inc. Dba Avr Sonovation's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Sonovation, Inc. Dba Avr Sonovation in the registry?
The most recently registered devices listed for Sonovation, Inc. Dba Avr Sonovation include EXTEND-EAR and MODEL FT40 TRANSONIC(TM) HEARING AID.