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Visus Technology Transfer GmbH

Country not established

Devices
3

What Visus Technology Transfer GmbH makes

Visus Technology Transfer GmbH develops medical imaging software, including the JiveX platform and its associated JiveX software solutions, designed for radiology workflows and diagnostic imaging analysis.

The company’s portfolio is regulated under FDA’s Class II device classification, with relevant products listed via the 510(k) premarket notification process. The manufacturer is based in the United States.

AI-generated from registry data, 2 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue3

Newest first, rows 1-3 of 3

  • JiveX Ref K162008

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Jive X Software Ref K053183

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • JiveX Ref K142750

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

Frequently asked questions

How many devices does Visus Technology Transfer GmbH have in the registry?

The registry currently lists 3 devices for Visus Technology Transfer GmbH. Devices recorded under merged duplicate company entries are counted once.

Which registries list Visus Technology Transfer GmbH's devices?

Among its 3 most recently registered devices, Visus Technology Transfer GmbH has devices listed in FDA 510(k) (3 devices).

What risk classes do Visus Technology Transfer GmbH's devices fall under?

Among its 3 most recently registered devices, the classes recorded for Visus Technology Transfer GmbH's devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Visus Technology Transfer GmbH in the registry?

The most recently registered devices listed for Visus Technology Transfer GmbH include JiveX and JIVE X SOFTWARE.

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