Maxant Technologies, Inc.
Country not established
- Devices
- 1
What Maxant Technologies, Inc. makes
Maxant Technologies, Inc. makes medical devices such as the MEDIPORT. These devices are categorized as Class II, indicating they are of moderate risk.
The company's portfolio is regulated and listed in the fda_510k registry, which is a database of medical devices that have been cleared for marketing in the US. Maxant Technologies, Inc. is based in the US.
Catalogue
Mediport Ref K060210
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Maxant Technologies, Inc. have in the registry?
The registry currently lists 1 device for Maxant Technologies, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Maxant Technologies, Inc.'s devices?
Among its 1 most recently registered device, Maxant Technologies, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Maxant Technologies, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Maxant Technologies, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Maxant Technologies, Inc. in the registry?
The most recently registered devices listed for Maxant Technologies, Inc. include MEDIPORT.