Motion Dynamics
CanadaFDA applicant, unverified
- Devices
- 1
What Motion Dynamics makes
Motion Dynamics manufactures the FYMCO FLYER, a device designed for dynamic lower-limb rehabilitation and gait training, intended to assist patients in restoring mobility through controlled movement exercises.
The FYMCO FLYER is classified as a Class II medical device in the US and is authorised through the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Fymco Flyer Ref K915416
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Motion Dynamics have in the registry?
The registry currently lists 1 device for Motion Dynamics. Devices recorded under merged duplicate company entries are counted once.
Which registries list Motion Dynamics's devices?
Among its 1 most recently registered device, Motion Dynamics has devices listed in FDA 510(k) (1 device).
What risk classes do Motion Dynamics's devices fall under?
Among its 1 most recently registered device, the classes recorded for Motion Dynamics's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Motion Dynamics in the registry?
The most recently registered devices listed for Motion Dynamics include FYMCO FLYER.