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Koag, LLC

Country not established

Devices
1

What Koag, LLC makes

Koag, LLC manufactures the Vascette HP, a hemostatic pad designed to control bleeding by promoting rapid clotting at wound sites.

The Vascette HP 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, 2 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • Vascette HP (hemostatic pad) Ref K220566

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

Frequently asked questions

How many devices does Koag, LLC have in the registry?

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

Which registries list Koag, LLC's devices?

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

What are the newest devices from Koag, LLC in the registry?

The most recently registered devices listed for Koag, LLC include Vascette HP (hemostatic pad).

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