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Remedium Technologies, Inc.

Country not established

Devices
1

What Remedium Technologies, Inc. makes

Remedium Technologies, Inc. manufactures the Hemogrip Patch, a medical adhesive designed to secure vascular access devices such as catheters and ports to the skin.

The Hemogrip Patch is classified as a Class II (U) device in the U.S. and is listed under the FDA’s 510(k) pathway. 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

  • Hemogrip Patch Ref K143466

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

Frequently asked questions

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

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

Which registries list Remedium Technologies, Inc.'s devices?

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

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

The most recently registered devices listed for Remedium Technologies, Inc. include Hemogrip Patch.

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