Smh Biomaterial AG
Country not established
- Devices
- 1
What Smh Biomaterial AG makes
Smh Biomaterial AG makes the SMH FLEX S device.
The SMH FLEX S is a Class II medical device listed in the FDA 510(k) registry, and the company is based in the United States.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Smh Flex S Ref K073040
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Smh Biomaterial AG have in the registry?
The registry currently lists 1 device for Smh Biomaterial AG. Devices recorded under merged duplicate company entries are counted once.
Which registries list Smh Biomaterial AG's devices?
Among its 1 most recently registered device, Smh Biomaterial AG has devices listed in FDA 510(k) (1 device).
What risk classes do Smh Biomaterial AG's devices fall under?
Among its 1 most recently registered device, the classes recorded for Smh Biomaterial AG's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Smh Biomaterial AG in the registry?
The most recently registered devices listed for Smh Biomaterial AG include SMH FLEX S.