I-Motion Group Global Iberica S.L.
SpainFDA 510(k) applicant, unverified
- Devices
- 1
What I-Motion Group Global Iberica S.L. makes
I-Motion Group Global Iberica S.L. manufactures the I-Motion device, which is classified as a Class II medical device.
The company is based in the US and the I-Motion device is listed in the FDA 510(k) registry.
Catalogue
I-Motion Ref K212413
510(k) 510(k)
Frequently asked questions
How many devices does I-Motion Group Global Iberica S.L. have in the registry?
The registry currently lists 1 device for I-Motion Group Global Iberica S.L.. Devices recorded under merged duplicate company entries are counted once.
Which registries list I-Motion Group Global Iberica S.L.'s devices?
Among its 1 most recently registered device, I-Motion Group Global Iberica S.L. has devices listed in FDA 510(k) (1 device).
What risk classes do I-Motion Group Global Iberica S.L.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for I-Motion Group Global Iberica S.L.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from I-Motion Group Global Iberica S.L. in the registry?
The most recently registered devices listed for I-Motion Group Global Iberica S.L. include I-Motion.