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Churchill Corp.

United StatesFDA applicant, unverified

Devices
35

What Churchill Corp. makes

Churchill Corp. manufactures intravenous (IV) administration sets, including vented and non-vented designs with metering chambers, as well as extension tubes and luer lock caps for fluid pathways. Their portfolio also includes blood administration sets, blood gas sampler kits, and specialized sets for total parenteral nutrition (TPN) and nitroglycerine infusion. Bag-to-bag and bottle-to-bag transfer systems are also part of their product line.

The company’s devices are regulated under the FDA’s Class I and Class II classifications, with most products listed via the 510(k) pathway. These products are intended for use in the US and are subject to FDA oversight as medical devices. The manufacturer is based in the United States.

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 Churchill Corp. have in the registry?

The registry currently lists 35 devices for Churchill Corp.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Churchill Corp.'s devices?

Among its 35 most recently registered devices, Churchill Corp. has devices listed in FDA 510(k) (35 devices).

What risk classes do Churchill Corp.'s devices fall under?

Among its 35 most recently registered devices, the classes recorded for Churchill Corp.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from Churchill Corp. in the registry?

The most recently registered devices listed for Churchill Corp. include CHURCHILL HABER POINT NEEDLE ADMIN. SET, CHURCHILL-HS SUSPENDED NON-VENTED IV SET, CHURCHILL-H EXTENSION TUBE and CHURCHILL BLOOD ADMINISTRATION SET.

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