Medivision (U.S.A.), Inc.
Country not established
- Devices
- 1
What Medivision (U.S.A.), Inc. makes
Medivision (U.S.A.), Inc. manufactures the Medivision IGS System, a device designed for intraoperative imaging guidance, enabling real-time visualization during surgical procedures to enhance precision and accuracy.
The company’s portfolio is regulated under Class II devices in the U.S., with the Medivision IGS System authorised via the FDA’s 510(k) clearance process. The company is based in the United States.
Catalogue
Medivision Igs System Ref K003699
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Medivision (U.S.A.), Inc. have in the registry?
The registry currently lists 1 device for Medivision (U.S.A.), Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medivision (U.S.A.), Inc.'s devices?
Among its 1 most recently registered device, Medivision (U.S.A.), Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Medivision (U.S.A.), Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Medivision (U.S.A.), Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Medivision (U.S.A.), Inc. in the registry?
The most recently registered devices listed for Medivision (U.S.A.), Inc. include MEDIVISION IGS SYSTEM.