Somedic AB
Country not established
- Devices
- 1
What Somedic AB makes
Somedic AB manufactures the VIBRAMETER, which is a device used for sensory testing.
The company is based in the US, and its product is classified as a Class I device listed in the FDA 510(k) registry.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Vibrameter Ref K843486
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Somedic AB have in the registry?
The registry currently lists 1 device for Somedic AB. Devices recorded under merged duplicate company entries are counted once.
Which registries list Somedic AB's devices?
Among its 1 most recently registered device, Somedic AB has devices listed in FDA 510(k) (1 device).
What risk classes do Somedic AB's devices fall under?
Among its 1 most recently registered device, the classes recorded for Somedic AB's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Somedic AB in the registry?
The most recently registered devices listed for Somedic AB include VIBRAMETER.