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Aircast, Inc.

United StatesFDA applicant, unverified

Devices
11

What Aircast, Inc. makes

Aircast, Inc. manufactures pneumatic compression devices, including systems like the VenaFlow and ArterialFlow for venous and arterial circulation support, as well as accessories such as the AutoChill kit and reusable/sterile cuffs. Their portfolio also includes braces like the Airstirrup Ankle Brace and Knee Brace, along with specialized products such as the EdemaFlow System and a tennis arm band for localized compression therapy.

The company’s devices are classified under FDA’s Class I and Class II categories, with most requiring 510(k) clearance. These products are listed in the FDA’s 510(k) registry, reflecting their regulatory status in the United States.

AI-generated from registry data, 2 Oct 2026. Not verified by deviCERTS or the manufacturer.

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Frequently asked questions

How many devices does Aircast, Inc. have in the registry?

The registry currently lists 11 devices for Aircast, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Aircast, Inc.'s devices?

Among its 11 most recently registered devices, Aircast, Inc. has devices listed in FDA 510(k) (11 devices).

What risk classes do Aircast, Inc.'s devices fall under?

Among its 11 most recently registered devices, the classes recorded for Aircast, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from Aircast, Inc. in the registry?

The most recently registered devices listed for Aircast, Inc. include VENAFLOW SYSTEM, MODEL 30A, ARTERIALFLOW SYSTEM, MODEL 32A, AUTOCHILL ACCESSORY KIT and AIRCAST VENAFLOW SYSTEM (MODIFICATION).

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