Somatronics, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Somatronics, Inc. makes
Somatronics, Inc. manufactures electrical nerve stimulators, including the Myotron, which delivers targeted nerve stimulation for therapeutic applications.
These devices are classified as Class II under FDA regulations and are listed in the 510(k) registry. The company is based in the United States.
Catalogue
Stimulator, Electrical Nerve Ref K782127
Regimes: 510(k) Registry: 510(k)Myotron Ref K761350
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Somatronics, Inc. have in the registry?
The registry currently lists 2 devices for Somatronics, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Somatronics, Inc.'s devices?
Among its 2 most recently registered devices, Somatronics, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Somatronics, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Somatronics, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Somatronics, Inc. in the registry?
The most recently registered devices listed for Somatronics, Inc. include STIMULATOR, ELECTRICAL NERVE and MYOTRON.