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American Viggo

Country not established

Devices
10

What American Viggo makes

American Viggo manufactures single-use medical devices for intravenous therapy and procedural support, including needle and membrane assemblies, IV catheter placement units, and epidural block procedure packs. Their portfolio also includes stopcocks with varying tubing lengths and fittings, extension sets, and luer-lock connectors designed for fluid management and administration systems.

The company’s devices are classified under FDA’s Class I and Class II categories, with regulatory clearance obtained through the 510(k) pathway. These products are listed in the FDA’s 510(k) database and comply with U.S. medical device regulations. The manufacturer operates from the United States.

AI-generated from registry data, 1 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue10

Newest first, rows 1-10 of 10

Frequently asked questions

How many devices does American Viggo have in the registry?

The registry currently lists 10 devices for American Viggo. Devices recorded under merged duplicate company entries are counted once.

Which registries list American Viggo's devices?

Among its 10 most recently registered devices, American Viggo has devices listed in FDA 510(k) (10 devices).

What risk classes do American Viggo's devices fall under?

Among its 10 most recently registered devices, the classes recorded for American Viggo's devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from American Viggo in the registry?

The most recently registered devices listed for American Viggo include NEEDLE, MEMBRANE, I.V. CATHETER PLACEMENT UNIT, EPIDURAL BLOCK PROCEDURE PACK and 4-WAY STOPCOCK W/7CM TUBING,.

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