Pmx, Inc.
Country not established
- Devices
- 1
What Pmx, Inc. makes
Pmx, Inc. manufactures the MediOMx, a medical device designed for [specific clinical application or function—if unspecified, omit detail and generalize]: [e.g., 'diagnostic imaging, monitoring, or therapeutic interventions in [relevant specialty]'].
The MediOMx is classified as a Class II device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
MediOMx Ref K233331
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Pmx, Inc. have in the registry?
The registry currently lists 1 device for Pmx, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Pmx, Inc.'s devices?
Among its 1 most recently registered device, Pmx, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Pmx, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Pmx, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Pmx, Inc. in the registry?
The most recently registered devices listed for Pmx, Inc. include MediOMx.