Rehab, Inc.
Country not established
- Devices
- 1
What Rehab, Inc. makes
Rehab, Inc. manufactures a lateral flexion machine, a device designed to assist in measuring or improving spinal mobility through controlled range-of-motion exercises.
The company’s products fall under FDA Class I devices and are listed via the 510(k) pathway. The manufacturer is based in the United States.
Catalogue
Lateral Flexion Machine Ref K940455
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Rehab, Inc. have in the registry?
The registry currently lists 1 device for Rehab, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Rehab, Inc.'s devices?
Among its 1 most recently registered device, Rehab, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Rehab, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Rehab, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Rehab, Inc. in the registry?
The most recently registered devices listed for Rehab, Inc. include LATERAL FLEXION MACHINE.