Crux Biomedical
Country not established
- Devices
- 2
What Crux Biomedical makes
Crux Biomedical makes the Crux Vena Cava Filter System, a medical device designed for placement in the inferior vena cava to prevent pulmonary embolism by capturing blood clots.
The Crux Vena Cava Filter System is classified as a Class II device and is listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
Crux Vena Cava Filter System Ref K122585
510(k) 510(k)Crux Vena Cava Filter System Ref K120402
510(k) 510(k)
Frequently asked questions
How many devices does Crux Biomedical have in the registry?
The registry currently lists 2 devices for Crux Biomedical. Devices recorded under merged duplicate company entries are counted once.
Which registries list Crux Biomedical's devices?
Among its 2 most recently registered devices, Crux Biomedical has devices listed in FDA 510(k) (2 devices).
What risk classes do Crux Biomedical's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Crux Biomedical's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Crux Biomedical in the registry?
The most recently registered devices listed for Crux Biomedical include CRUX VENA CAVA FILTER SYSTEM.