Data / Medical devices / United States / Wave Neuroscience
Wave Neuroscience: FDA-registered device maker in Newport Beach, CA, United States, 1 510(k) clearance
Wave Neuroscience is registered with the FDA (registration 3016873039) in Newport Beach, CA, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated June 3, 2026. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3016873039
- Address
- 1601 Dove St Ste 205, Newport Beach, CA, United States, 92660
- Owner or operator
- Wave Neuroscience (10096253)
- Roles
- Manufacturer
- First device listed
- August 8, 2026
- Registered through
- 2026
- Brand names listed
- MeRT System
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Transcranial Magnetic Stimulation System For Post Traumatic Stress Disorder (Ptsd) | SIG | 2 | Manufacturer | 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 |
|---|---|---|---|---|---|---|
| June 3, 2026 | K260402 | MeRT System | SIG | Substantially Equivalent | Wave Neuroscience | accessdata.fda.gov |
Updated June 3, 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.