Enspectra Health, Inc.
Country not established
- Devices
- 1
What Enspectra Health, Inc. makes
Enspectra Health, Inc. manufactures the VIO System (V-1000), a device designed for intraoperative imaging to visualize and guide surgical procedures, particularly in neurosurgery and spinal interventions.
The VIO System is classified as a Class II medical device in the US and is listed under FDA 510(k) clearance. The company is based in the United States.
Catalogue
VIO System (V-1000) Ref K232789
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Enspectra Health, Inc. have in the registry?
The registry currently lists 1 device for Enspectra Health, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Enspectra Health, Inc.'s devices?
Among its 1 most recently registered device, Enspectra Health, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Enspectra Health, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Enspectra Health, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Enspectra Health, Inc. in the registry?
The most recently registered devices listed for Enspectra Health, Inc. include VIO System (V-1000).