Data / Medical devices / Transcranial Magnetic Stimulator / United States
FDA-registered makers of Transcranial Magnetic Stimulator in the United States: 8 establishments
8 establishments in the United States are registered with the FDA to make Transcranial Magnetic Stimulator (product code OBP). 3 have a 510(k) clearance or PMA approval on file and 1 has a recall event. FDA data exported November 2, 2026.
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- Device
- Transcranial Magnetic Stimulator
- Product code
- OBP
- Country
- United States
Makers of Transcranial Magnetic Stimulator in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Neuronetics Inc. | Malvern, PA, United States | Complaint file establishment, Manufacturer, Specification developer | 10 | March 22, 2024 | 0 | 2 | 0 | api.fda.gov |
| Magnus Medical Inc. | Burlingame, CA, United States | Manufacturer | 1 | September 1, 2022 | 0 | 0 | 0 | api.fda.gov |
| Neuromodulatory Devices & Applications (nmda), Inc | San Diego, CA, United States | Complaint file establishment, Manufacturer, Specification developer | 1 | June 27, 2025 | 0 | 0 | 0 | api.fda.gov |
| D&K Engineering | San Diego, CA, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Domico Med-Device, LLC | Fenton, MI, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Kuro Medical | Eden Prairie, MN, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Molex LLC | Naperville, IL, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Spartronics Strongsville, Inc. | Strongsville, OH, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated November 2, 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.