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Data / Medical devices / Analyzer, Gas, Carbon-Dioxide, Gaseous-Phase / Japan

FDA-registered makers of Analyzer, Gas, Carbon-Dioxide, Gaseous-Phase in Japan: 7 establishments

7 establishments in Japan are registered with the FDA to make Analyzer, Gas, Carbon-Dioxide, Gaseous-Phase (product code CCK). 5 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.

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Device
Analyzer, Gas, Carbon-Dioxide, Gaseous-Phase
Product code
CCK
Country
Japan

Makers of Analyzer, Gas, Carbon-Dioxide, Gaseous-Phase in Japan

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Nihon Kohden Corp.SHINJUKU-KU Tokyo, JapanSpecification developer11June 10, 2025000api.fda.gov
Nihon Kohden Corporation - Tokorozawa establishment Advanced Technology CenterTokorozawa Saitama, JapanComplaint file establishment, Specification developer10June 10, 2025000api.fda.gov
Nihon Kohden Tomioka Production CenterTOMIOKA-SHI Gunma, JapanManufacturer6October 11, 2017000api.fda.gov
Nihon Kohden Tomioka Corporation Nihon Kohden Kawamoto Production CenterFukaya-Shi Saitama, JapanManufacturer5June 10, 2025000api.fda.gov
Nihon Kohden Tomioka CorporationGunma Tokyo, JapanManufacturer1July 25, 2002000api.fda.gov
Fukuda Denshi Co., Ltd.Shiroi-shi Chiba, JapanManufacturer0000api.fda.gov
Fukuda Denshi Co., Ltd.Bunkyo-ku Tokyo, JapanSpecification developer0000api.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.