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Data / Medical devices / Massager, Therapeutic, Electric / Japan

FDA-registered makers of Massager, Therapeutic, Electric in Japan: 6 establishments

6 establishments in Japan are registered with the FDA to make Massager, Therapeutic, Electric (product code ISA). 0 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
Massager, Therapeutic, Electric
Product code
ISA
Country
Japan

Makers of Massager, Therapeutic, Electric in Japan

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Atex Co., Ltd.Osaka, JapanComplaint file establishment, Contract manufacturer, Contract sterilizer, Exporter to the US, Foreign private label distributor, Manufacturer, Remanufacturer, Repackager or relabeler, Reprocessor, Specification developer0000api.fda.gov
Family Inada Co., Ltd. Daisen FactorySAIHAKU-GUN Tottori, JapanManufacturer0000api.fda.gov
Fuji Medical Instruments MFG. Co. Ltd.MINAMIKAWACHI-GUN Osaka, JapanExporter to the US, Manufacturer0000api.fda.gov
Maxell Izumi Co., Ltd.TAGAWA-GUN Fukuoka, JapanExporter to the US, Manufacturer0000api.fda.gov
MJ Company, Inc.Okayama, JapanManufacturer0000api.fda.gov
NIN Co.,Ltd.Daisen-cho, Saihaku-gun, Tottori, JapanExporter to the US, 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.