Modela AG
SwitzerlandFDA applicant, unverified
- Devices
- 1
What Modela AG makes
Modela AG manufactures the Basic and Dominant Flex, which are designed as orthopedic fixation devices for spinal stabilization, featuring flexible rods for surgical applications in the spine.
These devices are classified under Class II and are listed in the FDA’s 510(k) registry. The company is based in the United States.
Catalogue
Basic, Dominant Flex Ref K170329
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Modela AG have in the registry?
The registry currently lists 1 device for Modela AG. Devices recorded under merged duplicate company entries are counted once.
Which registries list Modela AG's devices?
Among its 1 most recently registered device, Modela AG has devices listed in FDA 510(k) (1 device).
What risk classes do Modela AG's devices fall under?
Among its 1 most recently registered device, the classes recorded for Modela AG's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Modela AG in the registry?
The most recently registered devices listed for Modela AG include Basic, Dominant Flex.