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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
- linkedin.com/company/aneuvo
- facebook.com/Aneuvo.company
- [email protected]
- Phone
- +1 424 256 2194
- PRRC Contact
- Amelia Striegel
- EUDAMED SRN
- US-MF-000041520
- FDA FEI Number
- —
- DUNS Number
- —
Catalogue (13)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| ReCure ® Electrode Pad ReCure ® Elektrodenpad Coussinet d’électrodes ReCure ® Electrodo ReCure ® Piastra elettrodi ReCure ® ReCure ® elektrodepad | PAD-003-02 | EUDAMED | Class IIb | Active |
| Electrodo ReCure | PAD-003 | EUDAMED | Class IIb | Active |
| ReCure Elektrodenpad | PAD-003 | EUDAMED | Class IIb | Active |
| ExaStim® Stimulationssystem | EXA-001 | EUDAMED | Class IIb | Active |
| ReCure ® Elektrodenpad, ReCure® elektrodepad, Coussinet d’électrodes ReCure® | PAD-003 | EUDAMED | Class IIb | Active |
| Sistema de estimulación ExaStim | EXA-001 | EUDAMED | Class IIb | Active |
| Coussinet d’électrodes ReCure® | PAD-003 | EUDAMED | Class IIb | Active |
| Sistema di stimolazione ExaStim® | EXA-001 | EUDAMED | Class IIb | Active |
| ReCure® elektrodepad | PAD-003 | EUDAMED | Class IIb | Active |
| Piastra elettrodi ReCure | PAD-003 | EUDAMED | Class IIb | Active |
| ExaStim® stimulatiesysteem | EXA-001 | EUDAMED | Class IIb | Active |
| ExaStim Stimulationssystem | EXA-001 | EUDAMED | Class IIb | Active |
| Système de stimulation ExaStim® | EXA-001 | EUDAMED | Class IIb | Active |
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