3Dio
Country not established
- Devices
- 1
What 3Dio makes
3Dio manufactures the Lumos 3DX, a 3D imaging system designed for precise visualization of anatomical structures in medical procedures, particularly in orthopedic and spinal applications.
The Lumos 3DX is classified as a Class II medical device and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Lumos 3DX Ref K223780
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does 3Dio have in the registry?
The registry currently lists 1 device for 3Dio. Devices recorded under merged duplicate company entries are counted once.
Which registries list 3Dio's devices?
Among its 1 most recently registered device, 3Dio has devices listed in FDA 510(k) (1 device).
What risk classes do 3Dio's devices fall under?
Among its 1 most recently registered device, the classes recorded for 3Dio's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from 3Dio in the registry?
The most recently registered devices listed for 3Dio include Lumos 3DX.