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Clearline MD

Country not established

Devices
1

What Clearline MD makes

Clearline MD manufactures the ClearLine IV, a medical device designed for intravenous therapy administration, including fluid and medication delivery systems.

The ClearLine IV is classified as a Class II device under FDA regulations and is listed via 510(k) clearance. The company is based in the United States.

AI-generated from registry data, 3 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • ClearLine IV Ref K171954

    Active Regimes: 510(k) Registry: 510(k) Class:II

Frequently asked questions

How many devices does Clearline MD have in the registry?

The registry currently lists 1 device for Clearline MD. Devices recorded under merged duplicate company entries are counted once.

Which registries list Clearline MD's devices?

Among its 1 most recently registered device, Clearline MD has devices listed in FDA 510(k) (1 device).

What risk classes do Clearline MD's devices fall under?

Among its 1 most recently registered device, the classes recorded for Clearline MD's devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Clearline MD in the registry?

The most recently registered devices listed for Clearline MD include ClearLine IV.

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