Jupiter Endovascular
Country not established
- Devices
- 2
What Jupiter Endovascular makes
Jupiter Endovascular manufactures the Vertex™ Catheter, a vascular catheter intended for endovascular procedures.
The Vertex™ Catheter is classified as a Class II medical device and is listed in the FDA 510(k) registry. Jupiter Endovascular is based in the United States.
Catalogue
Vertex™ Thrombectomy System Ref K261523
510(k) 510(k)Vertex(TM) Catheter Ref K252027
510(k) 510(k)
Frequently asked questions
How many devices does Jupiter Endovascular have in the registry?
The registry currently lists 2 devices for Jupiter Endovascular. Devices recorded under merged duplicate company entries are counted once.
Which registries list Jupiter Endovascular's devices?
Among its 2 most recently registered devices, Jupiter Endovascular has devices listed in FDA 510(k) (2 devices).
What risk classes do Jupiter Endovascular's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Jupiter Endovascular's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Jupiter Endovascular in the registry?
The most recently registered devices listed for Jupiter Endovascular include Vertex™ Thrombectomy System and Vertex(TM) Catheter.