Arterial Vascular Engineering, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What Arterial Vascular Engineering, Inc. makes
Arterial Vascular Engineering, Inc. manufactures cardiovascular angiography catheters, including the AVE 4F SITESEER, and vascular support devices such as the GT1 FLOPPY, GT1 HI-PER FLEX, and GT1 LIGHT SUPPORT. The company also produces the AVE BRIDGE STENT SYSTEM, designed for vascular interventions.
These devices are classified under Class II by the FDA and are supported by 510(k) clearance records. The company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
GT1 Floppy, GT1 Hi-Per Flex, GT1 Light Support Ref K983927
Regimes: 510(k) Registry: 510(k)Ave Bridge Stent System Ref K971295
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Arterial Vascular Engineering, Inc. have in the registry?
The registry currently lists 3 devices for Arterial Vascular Engineering, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Arterial Vascular Engineering, Inc.'s devices?
Among its 3 most recently registered devices, Arterial Vascular Engineering, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Arterial Vascular Engineering, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Arterial Vascular Engineering, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Arterial Vascular Engineering, Inc. in the registry?
The most recently registered devices listed for Arterial Vascular Engineering, Inc. include AVE 4F SITESEER CARDIOVASCULAR ANGIOGRAPHIC CATHETER, GT1 FLOPPY, GT1 HI-PER FLEX, GT1 LIGHT SUPPORT and AVE BRIDGE STENT SYSTEM.