Charnwood Dynamics, Ltd.
United KingdomFDA applicant, unverified
- Devices
- 1
What Charnwood Dynamics, Ltd. makes
Charnwood Dynamics, Ltd. manufactures the CODA CX1 Motion Analysis System, a device designed for capturing and analyzing human movement data in clinical or research settings. This system is used to assess gait, joint kinematics, and biomechanical parameters for diagnostic or rehabilitative purposes.
The CODA CX1 Motion Analysis System is classified as a Class II medical device under FDA regulations and is listed in the FDA’s 510(k) database. The company is based in the United States.
Catalogue
Coda CX1 Motion Analysis System Ref K033514
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Charnwood Dynamics, Ltd. have in the registry?
The registry currently lists 1 device for Charnwood Dynamics, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Charnwood Dynamics, Ltd.'s devices?
Among its 1 most recently registered device, Charnwood Dynamics, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Charnwood Dynamics, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Charnwood Dynamics, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Charnwood Dynamics, Ltd. in the registry?
The most recently registered devices listed for Charnwood Dynamics, Ltd. include CODA CX1 MOTION ANALYSIS SYSTEM.