Rebox (UK), Ltd.
Country not established
- Devices
- 1
What Rebox (UK), Ltd. makes
Rebox (UK) Ltd. manufactures the REBOX II, a transcutaneous electrical nerve stimulation (TENS) device designed for pain management applications.
The REBOX II is classified as a Class II medical device and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Rebox Ii (Tens) Ref K895183
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Rebox (Uk), Ltd. have in the registry?
The registry currently lists 1 device for Rebox (Uk), Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Rebox (Uk), Ltd.'s devices?
Among its 1 most recently registered device, Rebox (Uk), Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Rebox (Uk), Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Rebox (Uk), Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Rebox (Uk), Ltd. in the registry?
The most recently registered devices listed for Rebox (Uk), Ltd. include REBOX II (TENS).