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Applied Vascular Devices, Inc.

United StatesFDA applicant, unverified

Devices
21

What Applied Vascular Devices, Inc. makes

Applied Vascular Devices, Inc. manufactures catheters and related access devices for surgical and diagnostic procedures, including operative cholangiographic catheters, irrigation catheters (4, 6, and 10 French), and introducer sheaths. Their portfolio also includes surgical trocars with seals, occlusion catheters, hemostasis valves, and disposable introducer sheaths. The company produces injectors with syringe handles and intrascular diagnostic catheters, designed for biliary and vascular applications.

The company’s devices are classified under FDA’s Class I and Class II categories, with regulatory submissions recorded in the FDA’s 510(k) database. These products are intended for use in the United States, where the manufacturer is based.

AI-generated from registry data, 3 Oct 2026. Not verified by deviCERTS or the manufacturer.

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Frequently asked questions

How many devices does Applied Vascular Devices, Inc. have in the registry?

The registry currently lists 21 devices for Applied Vascular Devices, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Applied Vascular Devices, Inc.'s devices?

Among its 21 most recently registered devices, Applied Vascular Devices, Inc. has devices listed in FDA 510(k) (21 devices).

What risk classes do Applied Vascular Devices, Inc.'s devices fall under?

Among its 21 most recently registered devices, the classes recorded for Applied Vascular Devices, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from Applied Vascular Devices, Inc. in the registry?

The most recently registered devices listed for Applied Vascular Devices, Inc. include OPERATIVE CHOLANGIOGRAPHIC CATHETER, SURGICAL TROCAR AND CANNULA, SURGICAL OBTURATOR WITH SEAL and INTIMAX(TM) IRRIGATION CATHETER.

Generated automatically from registry data and not verified by a human reviewer.