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Data / Medical devices / Full-Montage Standard Electroencephalograph / Japan

FDA-registered makers of Full-Montage Standard Electroencephalograph in Japan: 5 establishments

5 establishments in Japan are registered with the FDA to make Full-Montage Standard Electroencephalograph (product code GWQ). 4 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 3, 2026.

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Device
Full-Montage Standard Electroencephalograph
Product code
GWQ
Country
Japan

Makers of Full-Montage Standard Electroencephalograph in Japan

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Nihon Kohden Corp.SHINJUKU-KU Tokyo, JapanSpecification developer4August 25, 2017000api.fda.gov
Nihon Kohden Tomioka Production CenterTOMIOKA-SHI Gunma, JapanManufacturer4August 25, 2017000api.fda.gov
Nihon Kohden Corporation - Tokorozawa establishment Advanced Technology CenterTokorozawa Saitama, JapanComplaint file establishment, Specification developer3August 25, 2017000api.fda.gov
Nihon Kohden Tomioka CorporationGunma Tokyo, JapanManufacturer1July 29, 2011000api.fda.gov
Nihon Vinyl Cord Corporation - Kodama Second FactoryHonjo-shi Saitama, JapanContract manufacturer0000api.fda.gov

Updated November 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.