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Gvp Elettronica SRL

Country not established

Devices
1

What Gvp Elettronica SRL makes

Gvp Elettronica Srl manufactures the DM-EMG, a device designed for electromyography (EMG) testing to assess muscle and nerve function through electrical signal analysis.

The DM-EMG is classified as a Class II medical device and is listed under the FDA’s 510(k) premarket notification process. 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

  • Dm-Emg Ref K072513

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

Frequently asked questions

How many devices does Gvp Elettronica Srl have in the registry?

The registry currently lists 1 device for Gvp Elettronica Srl. Devices recorded under merged duplicate company entries are counted once.

Which registries list Gvp Elettronica Srl's devices?

Among its 1 most recently registered device, Gvp Elettronica Srl has devices listed in FDA 510(k) (1 device).

What risk classes do Gvp Elettronica Srl's devices fall under?

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

What are the newest devices from Gvp Elettronica Srl in the registry?

The most recently registered devices listed for Gvp Elettronica Srl include DM-EMG.

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