Data / Medical devices / United States / Aneuvo
Aneuvo: FDA-registered device maker in Los Angeles, CA, United States, 1 510(k) clearance
Aneuvo is registered with the FDA (registration 3045321552) in Los Angeles, CA, United States. It lists 2 device types. The FDA files 1 510(k) clearance under its listings, the newest dated March 27, 2026. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3045321552
- Address
- 10940 Wilshire Blvd Ste 2030, Los Angeles, CA, United States, 90024
- Owner or operator
- Aneuvo (10095773)
- Roles
- Complaint file establishment, Repackager or relabeler, Specification developer
- First device listed
- April 27, 2026
- Registered through
- 2026
- Brand names listed
- ExaStim, ReCure
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Electrode, Cutaneous | GXY | 2 | Complaint file establishment, Repackager or relabeler, Specification developer | accessdata.fda.gov |
| Transcutaneous Electrical Spine Stimulator To Improve Skeletal Muscle Strength And Sensation | SDO | 2 | Complaint file establishment, Repackager or relabeler, Specification developer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| March 27, 2026 | K252893 | ExaStim® Stimulation System (EXA-001); ExaStim® Stimulation System (EXA-011); ReCure® Electrode Pad (PAD-003); ReCure® Electrode Pad (PAD-013) | SDO | Substantially Equivalent | Aneuvo | accessdata.fda.gov |
Compare with other makers
- All makers of Electrode, Cutaneous
- All makers of Transcutaneous Electrical Spine Stimulator To Improve Skeletal Muscle Strength And Sensation
Updated March 27, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.