Medical Templates AG
SwitzerlandFDA applicant, unverified
- Devices
- 1
What Medical Templates AG makes
Medical Templates AG manufactures the Cube Navigator, a medical imaging navigation system designed for surgical planning and guidance in orthopedic procedures.
The Cube Navigator is classified as a Class II device and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Cube Navigator Ref K240620
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Medical Templates AG have in the registry?
The registry currently lists 1 device for Medical Templates AG. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medical Templates AG's devices?
Among its 1 most recently registered device, Medical Templates AG has devices listed in FDA 510(k) (1 device).
What risk classes do Medical Templates AG's devices fall under?
Among its 1 most recently registered device, the classes recorded for Medical Templates AG's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Medical Templates AG in the registry?
The most recently registered devices listed for Medical Templates AG include Cube Navigator.