Tinnitus Control, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Tinnitus Control, Inc. makes
Tinnitus Control, Inc. manufactures hearing aids designed to manage chronic tinnitus, including the Tinnitus RX and Tinnitus Phase-Out devices. These products use sound therapy and masking techniques to help reduce the perception of ringing or noise in the ears.
The company’s portfolio is regulated as Class II medical devices in the US, with devices listed under the FDA’s 510(k) clearance pathway. The manufacturer is based in the United States.
Catalogue
Tinnitus Rx Ref K031624
Regimes: 510(k) Registry: 510(k)Tinnitus Phase-Out Ref K061111
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Tinnitus Control, Inc. have in the registry?
The registry currently lists 2 devices for Tinnitus Control, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Tinnitus Control, Inc.'s devices?
Among its 2 most recently registered devices, Tinnitus Control, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Tinnitus Control, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Tinnitus Control, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Tinnitus Control, Inc. in the registry?
The most recently registered devices listed for Tinnitus Control, Inc. include TINNITUS RX and TINNITUS PHASE-OUT.