Cybernius Medical, Ltd.
CanadaFDA 510(k) applicant, unverified
- Devices
- 1
What Cybernius Medical, Ltd. makes
Cybernius Medical, Ltd. manufactures the CYBERREN, a medical device designed for renal denervation therapy to treat resistant hypertension.
The CYBERREN is classified as a Class II device under FDA regulations and is listed in the FDA’s 510(k) registry. The company is based in the United States.
Catalogue
Cyberren Ref K970989
510(k) 510(k)
Frequently asked questions
How many devices does Cybernius Medical, Ltd. have in the registry?
The registry currently lists 1 device for Cybernius Medical, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cybernius Medical, Ltd.'s devices?
Among its 1 most recently registered device, Cybernius Medical, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Cybernius Medical, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Cybernius Medical, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Cybernius Medical, Ltd. in the registry?
The most recently registered devices listed for Cybernius Medical, Ltd. include CYBERREN.