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3M Avi, Inc.

United StatesFDA applicant, unverified

Devices
18

What 3M Avi, Inc. makes

3M Avi, Inc. manufactures infusion pumps and related intravenous administration sets, including dual-channel and syringe pumps, volumetric pumps, and piggyback IV admin sets with manifold check valves.

The devices are classified as Class II medical devices and are listed in the FDA 510(k) registry; the company is based in the United States.

AI-generated from registry data, 30 Sep 2026. Not verified by deviCERTS or the manufacturer.

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Frequently asked questions

How many devices does 3M Avi, Inc. have in the registry?

The registry currently lists 18 devices for 3M Avi, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list 3M Avi, Inc.'s devices?

Among its 18 most recently registered devices, 3M Avi, Inc. has devices listed in FDA 510(k) (18 devices).

What risk classes do 3M Avi, Inc.'s devices fall under?

Among its 18 most recently registered devices, the classes recorded for 3M Avi, Inc.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from 3M Avi, Inc. in the registry?

The most recently registered devices listed for 3M Avi, Inc. include AVI MODEL 4225 VENTED PIGGYBACK IV ADMIN SET, AVI MODEL 870 DUAL CHANNEL INFUSION PUMP, AVI MICRO 285CM INFUSION PUMP and AVI MODEL 270CM INFUSION PUMP.

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