Maxima Intl., Inc.
Country not established
- Devices
- 1
What Maxima Intl., Inc. makes
Maxima Intl., Inc. manufactures the ULTRA 2000, a transcutaneous electrical nerve stimulation (T.E.N.S.) device designed for pain management applications.
The ULTRA 2000 is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Ultra 2000 (T.E.N.S.) Ref K884833
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Maxima Intl., Inc. have in the registry?
The registry currently lists 1 device for Maxima Intl., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Maxima Intl., Inc.'s devices?
Among its 1 most recently registered device, Maxima Intl., Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Maxima Intl., Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Maxima Intl., Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Maxima Intl., Inc. in the registry?
The most recently registered devices listed for Maxima Intl., Inc. include ULTRA 2000 (T.E.N.S.).