Redplane AG
SwitzerlandFDA applicant, unverified
- Devices
- 1
What Redplane AG makes
Redplane AG manufactures the ELEXOMA MEDIC, a medical device designed for targeted tissue ablation or treatment procedures.
The ELEXOMA MEDIC is classified as a Class II device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
Elexoma Medic Ref K070412
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Redplane AG have in the registry?
The registry currently lists 1 device for Redplane AG. Devices recorded under merged duplicate company entries are counted once.
Which registries list Redplane AG's devices?
Among its 1 most recently registered device, Redplane AG has devices listed in FDA 510(k) (1 device).
What risk classes do Redplane AG's devices fall under?
Among its 1 most recently registered device, the classes recorded for Redplane AG's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Redplane AG in the registry?
The most recently registered devices listed for Redplane AG include ELEXOMA MEDIC.