Medivision Endoscopy
Country not established
- Devices
- 1
What Medivision Endoscopy makes
Medivision Endoscopy manufactures the I-View Personal Video Display, a handheld device designed for real-time visualization during endoscopic procedures, enabling clinicians to view internal imaging directly at the procedure site.
The I-View Personal Video Display 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
Medivision I-View Personal Video Display Ref K000669
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Medivision Endoscopy have in the registry?
The registry currently lists 1 device for Medivision Endoscopy. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medivision Endoscopy's devices?
Among its 1 most recently registered device, Medivision Endoscopy has devices listed in FDA 510(k) (1 device).
What risk classes do Medivision Endoscopy's devices fall under?
Among its 1 most recently registered device, the classes recorded for Medivision Endoscopy's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Medivision Endoscopy in the registry?
The most recently registered devices listed for Medivision Endoscopy include MEDIVISION I-VIEW PERSONAL VIDEO DISPLAY.