Rehabilitation Technologies Division
Country not established
- Devices
- 1
What Rehabilitation Technologies Division makes
The company produces the RTD ARM Assistive Robotic Device, a robotic system designed to support and enhance upper-limb mobility and function for users requiring assistive rehabilitation.
This device is classified as Class II under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The manufacturer is based in the United States.
Catalogue
Rtd Arm Assistive Robotic Device Ref K993443
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Rehabilitation Technologies Division have in the registry?
The registry currently lists 1 device for Rehabilitation Technologies Division. Devices recorded under merged duplicate company entries are counted once.
Which registries list Rehabilitation Technologies Division's devices?
Among its 1 most recently registered device, Rehabilitation Technologies Division has devices listed in FDA 510(k) (1 device).
What risk classes do Rehabilitation Technologies Division's devices fall under?
Among its 1 most recently registered device, the classes recorded for Rehabilitation Technologies Division's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Rehabilitation Technologies Division in the registry?
The most recently registered devices listed for Rehabilitation Technologies Division include RTD ARM ASSISTIVE ROBOTIC DEVICE.