Magnevu
Country not established
- Devices
- 1
What Magnevu makes
Magnevu manufactures the ORTHOVU-1000, a medical device designed for orthopedic imaging and navigation, likely used in surgical planning or intraoperative guidance for spinal or joint procedures.
The ORTHOVU-1000 is classified as a Class II device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
Orthovu-1000 Ref K981898
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Magnevu have in the registry?
The registry currently lists 1 device for Magnevu. Devices recorded under merged duplicate company entries are counted once.
Which registries list Magnevu's devices?
Among its 1 most recently registered device, Magnevu has devices listed in FDA 510(k) (1 device).
What risk classes do Magnevu's devices fall under?
Among its 1 most recently registered device, the classes recorded for Magnevu's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Magnevu in the registry?
The most recently registered devices listed for Magnevu include ORTHOVU-1000.