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Rexaderm, Inc.

Country not established

Devices
1

What Rexaderm, Inc. makes

Rexaderm, Inc. manufactures the REXASTOM ORAL EASE, a device designed to facilitate oral care and reduce discomfort for patients with stomatitis or oral mucositis, particularly those undergoing chemotherapy or radiation therapy.

The REXASTOM ORAL EASE is classified as a Class II device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. 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

  • Rexastom Oral Ease Ref K082553

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

Frequently asked questions

How many devices does Rexaderm, Inc. have in the registry?

The registry currently lists 1 device for Rexaderm, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Rexaderm, Inc.'s devices?

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

What are the newest devices from Rexaderm, Inc. in the registry?

The most recently registered devices listed for Rexaderm, Inc. include REXASTOM ORAL EASE.

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