Imidex, Inc.
Country not established
- Devices
- 1
What Imidex, Inc. makes
Imidex, Inc. manufactures the VisiRad XR, a medical imaging device designed for real-time fluoroscopy and radiographic visualization, primarily used in interventional procedures.
The VisiRad XR 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
VisiRad XR Ref K223133
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Imidex, Inc. have in the registry?
The registry currently lists 1 device for Imidex, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Imidex, Inc.'s devices?
Among its 1 most recently registered device, Imidex, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Imidex, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Imidex, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Imidex, Inc. in the registry?
The most recently registered devices listed for Imidex, Inc. include VisiRad XR.