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Exodus Innovations

IsraelFDA 510(k) applicant, unverified

Devices
1

What Exodus Innovations makes

Exodus Innovations manufactures the ZIDA Wearable Neuromodulation System, a non-invasive device designed for neuromodulation therapy to address neurological conditions.

The ZIDA Wearable Neuromodulation System is classified as a Class II medical device and is listed under the FDA’s 510(k) pathway. The company is based in the United States.

AI-generated from registry data, 3 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

Frequently asked questions

How many devices does Exodus Innovations have in the registry?

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

Which registries list Exodus Innovations's devices?

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

What risk classes do Exodus Innovations's devices fall under?

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

What are the newest devices from Exodus Innovations in the registry?

The most recently registered devices listed for Exodus Innovations include ZIDA Wearable Neuromodulation System.

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