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ANEUVO

United States·US-MF-000041520

Last updated September 18, 2026

About

ANEUVO has been featured by leading news networks, business and health podcasts, and science and research conferences around the world. Learn more about our company, our technology, and individuals’ experiences with transcutaneous spinal stimulation and the ExaStim Stimulation System in the stories below.

From the manufacturer's own website. Source

What ANEUVO makes

The company manufactures reusable electrode pads for transcutaneous spinal stimulation, including the ReCure® brand pads designed for medical use. It also produces the ExaStim® Stimulationssystem, a device intended for non-invasive spinal cord stimulation via external electrical stimulation.

These products fall under EU Class IIb medical device classifications and are registered in the EUDAMED database. The company is based in the United States.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What medical devices does ANEUVO manufacture?

ANEUVO manufactures reusable electrode pads for transcutaneous spinal stimulation under the ReCure® brand, and the ExaStim® Stimulationssystem, a device for non-invasive spinal cord stimulation via external electrical stimulation.

Where is ANEUVO based?

ANEUVO is based in the United States, as indicated by the country information provided in the device data.

Which regulatory registries list ANEUVO's devices?

ANEUVO's devices are listed in the EUDAMED database, which is the European Union's medical device database, as specified in the device data.

How are ANEUVO's devices classified?

ANEUVO's devices are classified as Class IIb medical devices, which is a classification level indicating moderate risk, as stated in the device data.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
United States
Address
10940, Wilshire Blvd, Los Angeles, United States
Website
aneuvo.com
Phone
+1 424 256 2194
PRRC Contact
Amelia Striegel
EUDAMED SRN
US-MF-000041520
FDA FEI Number
—
DUNS Number
—

Catalogue (13)

DeviceModel / ReferenceRegistriesClassStatus
ReCure ® Electrode Pad ReCure ® Elektrodenpad Coussinet d’électrodes ReCure ® Electrodo ReCure ® Piastra elettrodi ReCure ® ReCure ® elektrodepad PAD-003-02
EUDAMED
Class IIbActive
Electrodo ReCure PAD-003
EUDAMED
Class IIbActive
ReCure Elektrodenpad PAD-003
EUDAMED
Class IIbActive
ExaStim® Stimulationssystem EXA-001
EUDAMED
Class IIbActive
ReCure ® Elektrodenpad, ReCure® elektrodepad, Coussinet d’électrodes ReCure® PAD-003
EUDAMED
Class IIbActive
Sistema de estimulación ExaStim EXA-001
EUDAMED
Class IIbActive
Coussinet d’électrodes ReCure® PAD-003
EUDAMED
Class IIbActive
Sistema di stimolazione ExaStim® EXA-001
EUDAMED
Class IIbActive
ReCure® elektrodepad PAD-003
EUDAMED
Class IIbActive
Piastra elettrodi ReCure PAD-003
EUDAMED
Class IIbActive
ExaStim® stimulatiesysteem EXA-001
EUDAMED
Class IIbActive
ExaStim Stimulationssystem EXA-001
EUDAMED
Class IIbActive
Système de stimulation ExaStim® EXA-001
EUDAMED
Class IIbActive

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