Cagent Vascular
Active in EUDAMEDUnited Statesfrom SRN EUDAMED FDA SRN US-MF-000012243 FEI 3014598164
- Devices
- 45
- Registrations
- EUDAMEDFDA
- FDA recalls
- 0
At a glance
Market reach
- European Union
- EUDAMED actor
- United States
- FDA FEI
Catalogue
Search and filter all 45 devicesCompany details
- EUDAMED SRN
- US-MF-000012243
- FDA FEI number
- 3014598164
- EUDAMED status
- Active
- EUDAMED registered name
- Cagent Vascular, Inc.
- Registered address
- 150, Strafford Avenue, 19087, Wayne, United States
- Website
- www.cagentvascular.com
- [email protected]
- PRRC contact
- Peter Johansson
Frequently asked questions
How many devices does CAGENT VASCULAR have in the registry?
The registry currently lists 45 devices for CAGENT VASCULAR. Devices recorded under merged duplicate company entries are counted once.
Which registries list CAGENT VASCULAR's devices?
Among its 45 most recently registered devices, CAGENT VASCULAR has devices listed in EUDAMED (20 devices), FDA 510(k) (5 devices) and FDA GUDID (20 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do CAGENT VASCULAR's devices fall under?
Among its 45 most recently registered devices, the classes recorded for CAGENT VASCULAR's devices are Class IIa and Class II. Each device page shows its own class and authorisation.
What are the newest devices from CAGENT VASCULAR in the registry?
The most recently registered devices listed for CAGENT VASCULAR include Serranator® PTA Serration Balloon Catheter, Serranator FGS-0898-7040, Serranator FGS-0898-8040 and Serranator SL-PRO.