Tinnitech, Ltd.
AustraliaFDA applicant, unverified
- Devices
- 1
What Tinnitech, Ltd. makes
Tinnitech, Ltd. manufactures the Acoustic Neuro Modulation Protocol (ANMP), which is a device designed for acoustic neuromodulation.
This device is classified as Class II and is listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
Anmp (Acoustic Neuro Modulation Protocol) Ref K030791
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Tinnitech, Ltd. have in the registry?
The registry currently lists 1 device for Tinnitech, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Tinnitech, Ltd.'s devices?
Among its 1 most recently registered device, Tinnitech, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Tinnitech, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Tinnitech, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Tinnitech, Ltd. in the registry?
The most recently registered devices listed for Tinnitech, Ltd. include ANMP (ACOUSTIC NEURO MODULATION PROTOCOL).