Vb Technologies AG
SwitzerlandFDA applicant, unverified
- Devices
- 1
What Vb Technologies AG makes
Vb Technologies AG manufactures the Visionbody, a medical imaging device designed for body composition analysis and health monitoring. This system provides quantitative assessments of muscle mass, fat distribution, and bone density through advanced imaging technology, supporting clinical and consumer health applications.
The Visionbody is classified as a Class II device under FDA regulations and is authorised via the 510(k) pathway. The company is based in the United States, and the device is listed in the FDA’s 510(k) registry.
Catalogue
Visionbody Ref K222386
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Vb Technologies AG have in the registry?
The registry currently lists 1 device for Vb Technologies AG. Devices recorded under merged duplicate company entries are counted once.
Which registries list Vb Technologies AG's devices?
Among its 1 most recently registered device, Vb Technologies AG has devices listed in FDA 510(k) (1 device).
What risk classes do Vb Technologies AG's devices fall under?
Among its 1 most recently registered device, the classes recorded for Vb Technologies AG's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Vb Technologies AG in the registry?
The most recently registered devices listed for Vb Technologies AG include Visionbody.