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Vmi Technologies

CanadaFDA 510(k) applicant, unverified

Devices
1

What Vmi Technologies makes

Vmi Technologies manufactures the ECHOVACS device.

The company is based in the US, and its portfolio includes Class II devices that are listed in the FDA 510(k) registry.

AI-generated from registry data, 25 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • Echovacs Ref K971776

    Class II
    Active 510(k) 510(k) II

Frequently asked questions

How many devices does Vmi Technologies have in the registry?

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

Which registries list Vmi Technologies's devices?

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

What risk classes do Vmi Technologies's devices fall under?

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

What are the newest devices from Vmi Technologies in the registry?

The most recently registered devices listed for Vmi Technologies include ECHOVACS.

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