Maxx Digm, Inc.
Country not established
- Devices
- 1
What Maxx Digm, Inc. makes
Maxx Digm, Inc. manufactures the Zmaxx T Series, a line of medical devices designed for diagnostic or therapeutic use in specific clinical applications, though exact device functions are not specified.
The company’s portfolio is regulated under Class II devices in the United States, with products listed via the FDA’s 510(k) clearance process. The manufacturer is based in the US.
Catalogue
Zmaxx T Series Ref K161219
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Maxx Digm, Inc. have in the registry?
The registry currently lists 1 device for Maxx Digm, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Maxx Digm, Inc.'s devices?
Among its 1 most recently registered device, Maxx Digm, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Maxx Digm, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Maxx Digm, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Maxx Digm, Inc. in the registry?
The most recently registered devices listed for Maxx Digm, Inc. include Zmaxx T Series.