Surgivisio
FranceFDA applicant, unverified
- Devices
- 1
What Surgivisio makes
Surgivisio manufactures the Surgivisio system, a medical device designed for intraoperative imaging and surgical guidance, enabling real-time visualization and precision during procedures.
The company’s portfolio is regulated under FDA Class II devices, with the Surgivisio system authorised via the 510(k) pathway. The device is listed in the FDA’s 510(k) registry. The manufacturer is based in the United States.
Catalogue
Surgivisio system Ref K202547
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Surgivisio have in the registry?
The registry currently lists 1 device for Surgivisio. Devices recorded under merged duplicate company entries are counted once.
Which registries list Surgivisio's devices?
Among its 1 most recently registered device, Surgivisio has devices listed in FDA 510(k) (1 device).
What risk classes do Surgivisio's devices fall under?
Among its 1 most recently registered device, the classes recorded for Surgivisio's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Surgivisio in the registry?
The most recently registered devices listed for Surgivisio include Surgivisio system.