Creative Fitness Developments S.L.
SpainFDA applicant, unverified
- Devices
- 1
What Creative Fitness Developments S.L. makes
Creative Fitness Developments S.L. manufactures the Gnesis EMS Plus, an electrical muscle stimulation (EMS) device designed for muscle activation and rehabilitation.
The Gnesis EMS Plus is classified as a Class II medical device and is listed under the FDA’s 510(k) pathway. The company is based in the US.
Catalogue
Gnesis EMS Plus Ref K230261
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Creative Fitness Developments S.L. have in the registry?
The registry currently lists 1 device for Creative Fitness Developments S.L.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Creative Fitness Developments S.L.'s devices?
Among its 1 most recently registered device, Creative Fitness Developments S.L. has devices listed in FDA 510(k) (1 device).
What risk classes do Creative Fitness Developments S.L.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Creative Fitness Developments S.L.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Creative Fitness Developments S.L. in the registry?
The most recently registered devices listed for Creative Fitness Developments S.L. include Gnesis EMS Plus.