Emjoi, Inc.
Country not established
- Devices
- 1
What Emjoi, Inc. makes
Emjoi, Inc. manufactures transcutaneous electrical nerve stimulation (TENS) devices designed for pain management, delivering low-voltage electrical pulses to the skin to alleviate discomfort.
The company’s TENS devices are classified as Class II under FDA regulations and are listed via the 510(k) clearance process. The portfolio is authorised for commercial distribution in the United States.
Catalogue
Emjoi Tens Device Ref K052711
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Emjoi, Inc. have in the registry?
The registry currently lists 1 device for Emjoi, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Emjoi, Inc.'s devices?
Among its 1 most recently registered device, Emjoi, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Emjoi, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Emjoi, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Emjoi, Inc. in the registry?
The most recently registered devices listed for Emjoi, Inc. include EMJOI TENS DEVICE.