Data / Medical devices / Tester, Electrode/Lead, Electroencephalograph
Tester, Electrode/Lead, Electroencephalograph (GYA): 6 FDA-registered makers in 3 countries
6 establishments in 3 countries are registered with the FDA to make Tester, Electrode/Lead, Electroencephalograph (product code GYA, Class 1, 21 CFR 882.1410). 0 of them have a 510(k) clearance or PMA approval on file and 0 have a recall event. The FDA has issued 5 510(k) clearances under this code, the latest on September 30, 1988, and lists 0 recall events (0 Class I). FDA data exported November 2, 2026.
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- Product code
- GYA
- Device class
- 1
- Regulation
- 882.1410
- Medical specialty
- Neurology
Makers by country
| Country | Makers |
|---|---|
| China | 2 |
| United States | 2 |
| Japan | 2 |
Makers of Tester, Electrode/Lead, Electroencephalograph
Registered establishments that manufacture, contract manufacture, remanufacture, reprocess or own the specification of this device, with the 510(k) clearances, PMA approvals and recalls the FDA files under each. Best documented first.
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| China Qingdao Bright Medical Manufacturing Co.,ltd. | Qingdao Shandong, China | Exporter to the US, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Netech Corp. | E Farmingdale, NY, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Neurofield, Inc. | Santa Barbara, CA, United States | Complaint file establishment, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Nihon Kohden Corp. | SHINJUKU-KU Tokyo, Japan | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Nihon Kohden Corporation - Tokorozawa establishment Advanced Technology Center | Tokorozawa Saitama, Japan | Complaint file establishment, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Wat Medical Technology Inc. | Ningbo Zhejiang, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated September 30, 1988. 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.