Aneuvo
Active in EUDAMEDUnited Statesfrom SRN EUDAMED FDA SRN US-MF-000041520 FEI 3045321552
- Devices
- 15
- Registrations
- EUDAMEDFDA
- FDA recalls
- 0
At a glance
EU certificates
1 of 1 in force.
Market reach
- European Union
- EUDAMED actor, 1 certificate
- United States
- FDA FEI
- Authorised rep.
- Obelis S.A.BE
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.
Catalogue
Search and filter all 15 devicesCompany details
- EUDAMED SRN
- US-MF-000041520
- FDA FEI number
- 3045321552
- EUDAMED status
- Active
- EUDAMED registered name
- ANEUVO
- Registered address
- 10940, Wilshire Blvd, 90024, Los Angeles, United States
- Website
- aneuvo.com
- linkedin.com/company/aneuvo
- facebook.com/Aneuvo.company
- Phone
- +1 424 256 2194
- PRRC contact
- Amelia Striegel
EUDAMED certificates
1 certificate1 valid, 0 expiredMDR 1next expiry 1 Apr 2030
DNV Product Assurance AS 2460 1 certificate
- C546374 Active
Quality management system EU MDR
- Issued
- 1 Apr 2025
- Expires
- 1 Apr 2030
From the company website
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.
Frequently asked questions
How many devices does ANEUVO have in the registry?
The registry currently lists 15 devices for ANEUVO. Devices recorded under merged duplicate company entries are counted once.
Which registries list ANEUVO's devices?
Among its 15 most recently registered devices, ANEUVO has devices listed in EUDAMED (15 devices).
What risk classes do ANEUVO's devices fall under?
Among its 15 most recently registered devices, the classes recorded for ANEUVO's devices are Class IIb. Each device page shows its own class and authorisation.
What EUDAMED certificates are recorded for ANEUVO?
EUDAMED lists 1 certificate for ANEUVO (quality management system) under MDR. 1 is recorded with the status issued. The most recent was issued on 1 Apr 2025.
What are the newest devices from ANEUVO in the registry?
The most recently registered devices listed for ANEUVO include ReCure® Electrode Pad, ReCure ® Electrode Pad ReCure ® Elektrodenpad Coussinet d’électrodes ReCure ® Electrodo ReCure ® Piastra elettrodi ReCure ® ReCure ® elektrodepad, Electrodo ReCure and ReCure Elektrodenpad.