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Data / Medical devices / Japan / Yamaha Motor Co Ltd

Yamaha Motor Co Ltd: FDA-registered device maker in Iwata Shizuoka, Japan, 3 510(k) clearances

Yamaha Motor Co Ltd is registered with the FDA (registration 3001185828) in Iwata Shizuoka, Japan. It lists 1 device type. The FDA files 3 510(k) clearances under its listings, the newest dated March 19, 2026. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
3001185828
Address
2500 Shingai, Iwata Shizuoka, Japan, 4388501
Owner or operator
YAMAHA MOTOR CO LTD (10047594)
Roles
Manufacturer
First device listed
October 9, 2014
Registered through
2026
Brand names listed
JWX-1 Plus (Navi Go 16 / Navi Go 24), JWX-2, NAVIGO2

Devices it lists

DeviceProduct codeClassRoleSource
Wheelchair, PoweredITI2Manufactureraccessdata.fda.gov

510(k) clearances

The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.

Decided510(k) numberDeviceProduct codeDecisionApplicantSource
March 19, 2026K252101JWG-1ITISubstantially EquivalentYamaha Motor Co., Ltd.accessdata.fda.gov
May 21, 2021K203806JWX-1 Plus (Navigo 16/Navigo 24)ITISubstantially EquivalentYamaha Motor Co., Ltd.accessdata.fda.gov
August 28, 2014K140204JWX-2ITISubstantially EquivalentYamaha Motor Co., Ltd.accessdata.fda.gov

Compare with other makers

Updated March 19, 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.