Arbor Endovascular
United Statesfrom the FDA registration address FDA establishment FEI 3039642752
- Devices
- 40
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
Search and filter all 40 devicesCompany details
- FDA FEI number
- 3039642752
- Address
- 2345 Bering Dr, San Jose, CA, 95131
Frequently asked questions
How many devices does ARBOR ENDOVASCULAR have in the registry?
The registry currently lists 40 devices for ARBOR ENDOVASCULAR. Devices recorded under merged duplicate company entries are counted once.
Which registries list ARBOR ENDOVASCULAR's devices?
Among its 40 most recently registered devices, ARBOR ENDOVASCULAR has devices listed in FDA 510(k) (5 devices) and FDA GUDID (35 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do ARBOR ENDOVASCULAR's devices fall under?
Among its 40 most recently registered devices, the classes recorded for ARBOR ENDOVASCULAR's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from ARBOR ENDOVASCULAR in the registry?
The most recently registered devices listed for ARBOR ENDOVASCULAR include Willow 14 Guidewire USTA14SO215S, Willow 14 Guidewire USTA14ST215S, Willow 14 Guidewire USTA14SU215S and Willow 14 Guidewire USTA14SO315S.