Neurotherapies Reset GmbH
GermanyFDA applicant, unverified
- Devices
- 1
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Neurotherapies Reset GmbH have in the registry?
The registry currently lists 1 device for Neurotherapies Reset GmbH. Devices recorded under merged duplicate company entries are counted once.
Which registries list Neurotherapies Reset GmbH's devices?
Among its 1 most recently registered device, Neurotherapies Reset GmbH has devices listed in FDA 510(k) (1 device).
What risk classes do Neurotherapies Reset GmbH's devices fall under?
Among its 1 most recently registered device, the classes recorded for Neurotherapies Reset GmbH's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Neurotherapies Reset GmbH in the registry?
The most recently registered devices listed for Neurotherapies Reset GmbH include Desyncra for Tinnitus Therapy System, Desyncra for Tinnitus Pro System.