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Ivs Solutions AG

GermanyFDA applicant, unverified

Devices
1

What Ivs Solutions AG makes

Ivs Solutions AG manufactures the CODIAGNOSTIX® 5.72, a diagnostic device designed for rapid and accurate medical testing, likely for point-of-care or laboratory use.

The company’s portfolio is regulated under Class II devices in the US, with the CODIAGNOSTIX® 5.72 listed via the FDA’s 510(k) pathway. The manufacturer 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

  • Codiagnostix (R) 5.72 Ref K071636

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

Frequently asked questions

How many devices does Ivs Solutions AG have in the registry?

The registry currently lists 1 device for Ivs Solutions AG. Devices recorded under merged duplicate company entries are counted once.

Which registries list Ivs Solutions AG's devices?

Among its 1 most recently registered device, Ivs Solutions AG has devices listed in FDA 510(k) (1 device).

What risk classes do Ivs Solutions AG's devices fall under?

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

What are the newest devices from Ivs Solutions AG in the registry?

The most recently registered devices listed for Ivs Solutions AG include CODIAGNOSTIX (R) 5.72.

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