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Data / Medical devices / Vehicle, Motorized 3-Wheeled / United States

FDA-registered makers of Vehicle, Motorized 3-Wheeled in the United States: 9 establishments

9 establishments in the United States are registered with the FDA to make Vehicle, Motorized 3-Wheeled (product code INI). 9 have a 510(k) clearance or PMA approval on file and 1 has a recall event. FDA data exported November 3, 2026.

SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.

Device
Vehicle, Motorized 3-Wheeled
Product code
INI
Country
United States

Makers of Vehicle, Motorized 3-Wheeled in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Pride Mobility Products Corp.North Las Vegas, NV, United StatesManufacturer10July 16, 2009000api.fda.gov
Pride Mobility Products Corp.Duryea, PA, United StatesManufacturer10July 16, 2009020api.fda.gov
Pride Mobility Products CorporationNorth Las Vegas, NV, United StatesManufacturer10July 16, 2009000api.fda.gov
Golden Brothers, Inc.Plains Township, PA, United StatesManufacturer, Specification developer4November 2, 2006000api.fda.gov
Pride Mobility Products CorporationPontotoc, MS, United StatesManufacturer4May 11, 2009000api.fda.gov
Electric MobilityCherry Hill, NJ, United StatesSpecification developer3June 8, 2026000api.fda.gov
Amigo Mobility Intl., Inc.Bridgeport, MI, United StatesManufacturer2July 30, 2010000api.fda.gov
Mega Motion, Inc.Duryea, PA, United StatesManufacturer1November 17, 2006000api.fda.gov
Metro Mobility Usa LLCMineola, NY, United StatesSpecification developer1July 19, 2023000api.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.