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Zinkh NV

BelgiumFDA 510(k) applicant, unverified

Devices
1

What Zinkh NV makes

Zinkh NV manufactures Elemental Granulate, a powdered medical formulation designed for oral administration, likely intended for nutritional or therapeutic supplementation.

The company’s portfolio is regulated under the FDA’s 510(k) pathway as a Class II device and is listed in the U.S. regulatory registry. Zinkh NV operates from 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

  • Elemental Granulate Ref K241283

    Unclassified
    Active 510(k) 510(k) —

Frequently asked questions

How many devices does Zinkh NV have in the registry?

The registry currently lists 1 device for Zinkh NV. Devices recorded under merged duplicate company entries are counted once.

Which registries list Zinkh NV's devices?

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

What are the newest devices from Zinkh NV in the registry?

The most recently registered devices listed for Zinkh NV include Elemental Granulate.

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