Data / Medical devices / Electrode, Cortical / United States
FDA-registered makers of Electrode, Cortical in the United States: 11 establishments
11 establishments in the United States are registered with the FDA to make Electrode, Cortical (product code GYC). 7 have a 510(k) clearance or PMA approval on file and 2 have a recall event. FDA data exported November 2, 2026.
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- Device
- Electrode, Cortical
- Product code
- GYC
- Country
- United States
Makers of Electrode, Cortical in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| PMT Corp. | Chanhassen, MN, United States | Manufacturer, Repackager or relabeler, Specification developer | 3 | May 8, 2009 | 0 | 0 | 0 | api.fda.gov |
| Ad-Tech Medical Instrument Corp. | Oak Creek, WI, United States | Manufacturer | 1 | January 25, 2020 | 0 | 2 | 1 | api.fda.gov |
| Blackrock Microsystems | Salt Lake City, UT, United States | Manufacturer | 1 | February 14, 2020 | 0 | 0 | 0 | api.fda.gov |
| Neuroone Medical Technologies Corp. | Eden Prairie, MN, United States | Complaint file establishment, Specification developer | 1 | November 26, 2019 | 0 | 0 | 0 | api.fda.gov |
| Nihon Kohden America, Inc. | Irvine, CA, United States | Complaint file establishment, Manufacturer | 1 | August 4, 2011 | 0 | 0 | 0 | api.fda.gov |
| Natus Neurology Incorporated | Middleton, WI, United States | Contract manufacturer, Specification developer | 1 | December 30, 2008 | 0 | 1 | 0 | api.fda.gov |
| Neuralynx, Inc. | Bozeman, MT, United States | Manufacturer | 1 | April 14, 2025 | 0 | 0 | 0 | api.fda.gov |
| Cadwell Industries, Inc. | Kennewick, WA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Cirtec Medical | Brooklyn Park, MN, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Ducommun LaBarge Technologies | Appleton, WI, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Qxmedical, LLC | Saint Paul, MN, 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.