Revital Lab, Inc.
Country not established
- Devices
- 1
What Revital Lab, Inc. makes
Revital Lab, Inc. develops the ZapStim Controller Application (Z1023), a device designed for transcutaneous electrical nerve stimulation (TENS) therapy to manage pain.
The ZapStim Controller Application is classified as a Class II medical device in the US and is authorised via the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
ZapStim Controller Application (Z1023) Ref K233631
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Revital Lab, Inc. have in the registry?
The registry currently lists 1 device for Revital Lab, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Revital Lab, Inc.'s devices?
Among its 1 most recently registered device, Revital Lab, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Revital Lab, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Revital Lab, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Revital Lab, Inc. in the registry?
The most recently registered devices listed for Revital Lab, Inc. include ZapStim Controller Application (Z1023).