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B. Braun of America, Inc.

United StatesFDA applicant, unverified

Devices
19

What B. Braun of America, Inc. makes

B. Braun of America, Inc. manufactures medical devices for intravenous therapy, vascular access, and diagnostic procedures, including subcutaneous injection sets, venous ports, fistula needles, and fluid transfer components. Their portfolio also includes cardiac output monitoring systems, biopsy tools, and specialized connectors like dispensing pins and chemo mini spikes.

These devices are classified under Class II in the U.S. and are listed via FDA 510(k) clearance. The company operates from 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 B. Braun of America, Inc. have in the registry?

The registry currently lists 19 devices for B. Braun of America, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list B. Braun of America, Inc.'s devices?

Among its 19 most recently registered devices, B. Braun of America, Inc. has devices listed in FDA 510(k) (19 devices).

What risk classes do B. Braun of America, Inc.'s devices fall under?

Among its 19 most recently registered devices, the classes recorded for B. Braun of America, Inc.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from B. Braun of America, Inc. in the registry?

The most recently registered devices listed for B. Braun of America, Inc. include TRUMPET VALVE, COMFORT-Q SUBCUTANEOUS INJECTION SETS, DUALTHERM(R) CARDIAC OUTPUT COMPUTER and CHARGED SUPOR(R) FILTER EXTENSION SET.

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