Cmed
Country not established
- Devices
- 2
What Cmed makes
Cmed manufactures the Stable Flow device, a medical instrument designed for precise fluid dynamics in clinical or procedural settings, and the Sensorimotor Rating Scale, a tool used to assess patient function and recovery in neurological or rehabilitation contexts.
The company’s portfolio includes Class I and Class II devices, regulated under the FDA’s 510(k) pathway, and is based in the United States.
Catalogue
Stable Flow Ref K981157
Regimes: 510(k) Registry: 510(k)Sensori-Motor Rating Scale Ref K946114
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Cmed have in the registry?
The registry currently lists 2 devices for Cmed. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cmed's devices?
Among its 2 most recently registered devices, Cmed has devices listed in FDA 510(k) (2 devices).
What risk classes do Cmed's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Cmed's devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Cmed in the registry?
The most recently registered devices listed for Cmed include STABLE FLOW and SENSORI-MOTOR RATING SCALE.