Electro Medical Development
Country not established
- Devices
- 1
What Electro Medical Development makes
Electro Medical Development manufactures the EMD TENZ pain control system. This device is designed to provide transcutaneous electrical nerve stimulation for the management of pain.
The company is based in the United States and its product portfolio is classified as Class II medical devices. The EMD TENZ pain control system is listed in the FDA 510(k) regulatory registry.
Catalogue
The Emd Tenz Pain Control System Ref K822841
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Electro Medical Development have in the registry?
The registry currently lists 1 device for Electro Medical Development. Devices recorded under merged duplicate company entries are counted once.
Which registries list Electro Medical Development's devices?
Among its 1 most recently registered device, Electro Medical Development has devices listed in FDA 510(k) (1 device).
What risk classes do Electro Medical Development's devices fall under?
Among its 1 most recently registered device, the classes recorded for Electro Medical Development's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Electro Medical Development in the registry?
The most recently registered devices listed for Electro Medical Development include THE EMD TENZ PAIN CONTROL SYSTEM.