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Flowtron-Aire, Ltd.

Country not established

Devices
1

What Flowtron-Aire, Ltd. makes

Flowtron-Aire, Ltd. manufactures intermittent pressure pads, which are designed to manage edema and promote lymphatic drainage in patients.

These devices are regulated under the FDA’s 510(k) clearance process and are listed in the U.S. market. The company is based in the United States.

AI-generated from registry data, 2 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • Intermittent Pressure Pad Ref K761227

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

Frequently asked questions

How many devices does Flowtron-Aire, Ltd. have in the registry?

The registry currently lists 1 device for Flowtron-Aire, Ltd.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Flowtron-Aire, Ltd.'s devices?

Among its 1 most recently registered device, Flowtron-Aire, Ltd. has devices listed in FDA 510(k) (1 device).

What are the newest devices from Flowtron-Aire, Ltd. in the registry?

The most recently registered devices listed for Flowtron-Aire, Ltd. include INTERMITTENT PRESSURE PAD.

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