Prosenex
Country not established
- Devices
- 1
What Prosenex makes
Prosenex makes medical devices such as the Dynamic Neuroscreening Device.
The company's portfolio, which includes Class I devices, is listed in the FDA 510k registry and is based in the US.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Dynamic Neuroscreening Device Ref K141208
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Prosenex have in the registry?
The registry currently lists 1 device for Prosenex. Devices recorded under merged duplicate company entries are counted once.
Which registries list Prosenex's devices?
Among its 1 most recently registered device, Prosenex has devices listed in FDA 510(k) (1 device).
What risk classes do Prosenex's devices fall under?
Among its 1 most recently registered device, the classes recorded for Prosenex's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Prosenex in the registry?
The most recently registered devices listed for Prosenex include DYNAMIC NEUROSCREENING DEVICE.