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Kipp & Zonen

Country not established

Devices
1

What Kipp & Zonen makes

Kipp & Zonen manufactures the ENDOMED 433, a medical device designed for endoscopic imaging and measurement within the gastrointestinal tract, enabling real-time visualization and data capture during procedures.

The ENDOMED 433 is classified under the FDA’s 510(k) pathway, indicating it is regulated as a Class II device. 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

  • Endomed 433 Ref K823362

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

Frequently asked questions

How many devices does Kipp & Zonen have in the registry?

The registry currently lists 1 device for Kipp & Zonen. Devices recorded under merged duplicate company entries are counted once.

Which registries list Kipp & Zonen's devices?

Among its 1 most recently registered device, Kipp & Zonen has devices listed in FDA 510(k) (1 device).

What are the newest devices from Kipp & Zonen in the registry?

The most recently registered devices listed for Kipp & Zonen include ENDOMED 433.

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