Tinnitus Treatment Centers, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Tinnitus Treatment Centers, Inc. makes
Tinnitus Treatment Centers, Inc. manufactures sound therapy devices, including pillow maskers and wearable ear devices designed to mask tinnitus symptoms. These products use low-level sound outputs to help users manage auditory perceptions, with variations in form factor such as full-size maskers, miniaturized ear units, and customizable frequency modules.
The company’s devices are classified as Class II under FDA regulations and are supported by 510(k) clearance records. The portfolio is listed in the FDA’s 510(k) database, and the manufacturer operates from the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Ttcghi-T And TTCTN3-T-T Ref K982451
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Tinnitus Treatment Centers, Inc. have in the registry?
The registry currently lists 2 devices for Tinnitus Treatment Centers, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Tinnitus Treatment Centers, Inc.'s devices?
Among its 2 most recently registered devices, Tinnitus Treatment Centers, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Tinnitus Treatment Centers, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Tinnitus Treatment Centers, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Tinnitus Treatment Centers, Inc. in the registry?
The most recently registered devices listed for Tinnitus Treatment Centers, Inc. include PILLOW MASKER, C2007M, C2008M, CE2000, WONDER EAR, MINI WONDER EAR, PT-2SM, PT-3SM, PT-3LFM, PT-3HFM, PT3CM, PT5-SM, PT5- and TTCGHI-T AND TTCTN3-T-T.