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Cleansite Medical, Inc.

Country not established

Devices
1

What Cleansite Medical, Inc. makes

Cleansite Medical, Inc. manufactures the ACTIV™ Cap, a medical device designed for wound care and infection prevention by promoting granulation tissue formation and reducing biofilm accumulation.

The ACTIV™ Cap is classified as a Class II device under FDA regulations and is supported by a 510(k) clearance. The company is based in the United States.

AI-generated from registry data, 1 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • ACTIV™ Cap Ref K223914

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

Frequently asked questions

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

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

Which registries list Cleansite Medical, Inc.'s devices?

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

What risk classes do Cleansite Medical, Inc.'s devices fall under?

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

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

The most recently registered devices listed for Cleansite Medical, Inc. include ACTIV™ Cap.

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