Vantis Vascular, Inc.
Country not established FDA establishment FEI 3032277090
- Devices
- 4
- Registrations
- FDA
- FDA recalls
- 0
What Vantis Vascular, Inc. makes
Vantis Vascular, Inc. manufactures vascular guide-catheters, which are single-use medical devices designed for interventional procedures.
The company's products, including the CrossFAST™ Integrated Microcatheter Advanced Delivery System and related devices, are classified as Class II and listed in the FDA 510(k) and FDA UDI registries. Vantis Vascular is based in the US.
Catalogue
- 510(k) 510(k)
- GUDID
- GUDID
- 510(k) 510(k)
Company details
- FDA FEI number
- 3032277090
- Address
- 2570 N 1st St Ste 200, San Jose, CA, 95131
Frequently asked questions
How many devices does VANTIS VASCULAR, INC. have in the registry?
The registry currently lists 4 devices for VANTIS VASCULAR, INC.. Devices recorded under merged duplicate company entries are counted once.
Which registries list VANTIS VASCULAR, INC.'s devices?
Among its 4 most recently registered devices, VANTIS VASCULAR, INC. has devices listed in FDA 510(k) (2 devices) and FDA GUDID (2 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do VANTIS VASCULAR, INC.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for VANTIS VASCULAR, INC.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from VANTIS VASCULAR, INC. in the registry?
The most recently registered devices listed for VANTIS VASCULAR, INC. include CrossFAST Integrated Microcatheter Advanced Delivery System, CrossFAST™ Integrated Microcatheter Advanced Delivery System CFM55, CrossFAST(TM) CFM55 and CrossFAST™ Integrated Microcatheter Guide Extension System (CFM55).