Scandiags AG
SwitzerlandFDA applicant, unverified
- Devices
- 1
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
ScanDiags Ortho L-Spine MR-Q Ref K242607
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Scandiags AG have in the registry?
The registry currently lists 1 device for Scandiags AG. Devices recorded under merged duplicate company entries are counted once.
Which registries list Scandiags AG's devices?
Among its 1 most recently registered device, Scandiags AG has devices listed in FDA 510(k) (1 device).
What risk classes do Scandiags AG's devices fall under?
Among its 1 most recently registered device, the classes recorded for Scandiags AG's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Scandiags AG in the registry?
The most recently registered devices listed for Scandiags AG include ScanDiags Ortho L-Spine MR-Q.