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Emsi

Also registered as Emsi, Inc.

Country not established

Devices
121

What Emsi makes

Emsi manufactures transcutaneous electrical stimulation electrodes, physical therapy transcutaneous neuromuscular electrical stimulation systems, knee support orthoses, and lumbar spine orthoses. Their specific products include the EMSI 40 x 40 Electrode, Hypoallergenic Electrode 2x2 4pk, Flex-TENS, Pro-Fit Knee Brace-Large Size, and various other electrode and brace models.

Emsi's devices are regulated as Class I and Class II medical devices and are listed in the FDA 510(k) and FDA UDI registries. The company is based in the United States.

AI-generated from registry data, 29 Sep 2026. Not verified by deviCERTS or the manufacturer.

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Company details

DUNS number
932471881

Frequently asked questions

How many devices does Emsi have in the registry?

The registry currently lists 121 devices for Emsi. Devices recorded under merged duplicate company entries are counted once.

Which registries list Emsi's devices?

Among its 50 most recently registered devices, Emsi has devices listed in FDA GUDID (50 devices).

What risk classes do Emsi's devices fall under?

Among its 50 most recently registered devices, the classes recorded for Emsi's devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from Emsi in the registry?

The most recently registered devices listed for Emsi include Hypoallergenic Electrode 2x2 4pk BF5050, EMSI 40 x 40 Electrode ELEC0012, Flex-TENS Retail 022017 FLET0001R02 and 25R(4)H-Samples SRELEC0001.

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