Avia Vascular
United Statesfrom the FDA registration address FDA FEI 3024537844
Avia Vascular is a medical device manufacturer, with 4 devices listed in FDA GUDID and FDA 510(k) (FDA Class II) as of 13 Nov 2026.
- Devices
- 4
- Registrations
- FDA
- FDA recalls
- 0
Registry facts
- Registries
- FDA GUDID 3
- FDA 510(k) 1
- Device classes
- FDA Class II 4
- Identifiers
- FDA FEI 3024537844
At a glance
Market reach
- United States
- FDA FEI
Catalogue
- Regimes: 510(k) Registry: GUDID
- Regimes: 510(k) Registry: GUDID
- Regimes: 510(k) Registry: GUDID
- Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3024537844
- Address
- 299 S Main St Ste 2300, Salt Lake City, UT, 84111
Frequently asked questions
How many devices does Avia Vascular have in the registry?
The registry currently lists 4 devices for Avia Vascular. Devices recorded under merged duplicate company entries are counted once.
Which registries list Avia Vascular's devices?
Among its 4 most recently registered devices, Avia Vascular has devices listed in FDA 510(k) (1 device) and FDA GUDID (3 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Avia Vascular's devices fall under?
Among its 4 most recently registered devices, the classes recorded for Avia Vascular's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Avia Vascular in the registry?
The most recently registered devices listed for Avia Vascular include 22G Open-System Ally Blood Collection Device AV110000, 20G Open-System Ally Blood Collection Device AV100000, 20G 8CM Stiletto Extended Dwell Catheter PIP200000 and 20G Open-System Ally Device Kit (AV100000), 22G Open-System Ally Device Kit (AV110000).