Neuromotion, Inc.
CanadaFDA applicant, unverified
- Devices
- 1
What Neuromotion, Inc. makes
Neuromotion, Inc. manufactures external functional neuromuscular stimulators, which are devices designed to stimulate muscles through electrical impulses to improve mobility or reduce atrophy in patients.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
External Functional Neuromuscular Stimulator Ref K974514
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Neuromotion, Inc. have in the registry?
The registry currently lists 1 device for Neuromotion, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Neuromotion, Inc.'s devices?
Among its 1 most recently registered device, Neuromotion, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Neuromotion, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Neuromotion, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Neuromotion, Inc. in the registry?
The most recently registered devices listed for Neuromotion, Inc. include EXTERNAL FUNCTIONAL NEUROMUSCULAR STIMULATOR.