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Data / Medical devices / Wheelchair, Powered / United States

FDA-registered makers of Wheelchair, Powered in the United States: 27 establishments

27 establishments in the United States are registered with the FDA to make Wheelchair, Powered (product code ITI). 23 have a 510(k) clearance or PMA approval on file and 6 have a recall event. FDA data exported November 2, 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.

Get makers of this device in the United StatesWatch these makers
Device
Wheelchair, Powered
Product code
ITI
Country
United States

Makers of Wheelchair, Powered in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Pride Mobility Products Corp.North Las Vegas, NV, United StatesManufacturer10May 12, 2022000api.fda.gov
Pride Mobility Products Corp.Duryea, PA, United StatesManufacturer10May 12, 2022040api.fda.gov
Pride Mobility Products CorporationNorth Las Vegas, NV, United StatesManufacturer10May 12, 2022000api.fda.gov
Sunrise Medical (us) LLCFresno, CA, United StatesComplaint file establishment, Specification developer10December 10, 2024050api.fda.gov
Sunrise Medical (US) LLCMount Juliet, TN, United StatesComplaint file establishment, Manufacturer10December 10, 2024000api.fda.gov
Merits Health Products, Inc.Las Vegas, NV, United StatesContract manufacturer, Repackager or relabeler8January 9, 2013000api.fda.gov
Merits Health Products., Inc.Fort Myers, FL, United StatesContract manufacturer, Repackager or relabeler8March 18, 2022010api.fda.gov
Permobil, Inc.Lebanon, TN, United StatesContract manufacturer, Manufacturer7March 27, 2015030api.fda.gov
Invacare Corp. Dba Invacare AmericaN Ridgeville, OH, United StatesComplaint file establishment, Manufacturer, Specification developer5March 19, 2021060api.fda.gov
Golden Brothers, Inc.Plains Township, PA, United StatesSpecification developer3March 22, 2007000api.fda.gov
Ki MobilityStevens Point, WI, United StatesManufacturer, Repackager or relabeler2January 10, 2025000api.fda.gov
Max Mobility, LLCLebanon, TN, United StatesComplaint file establishment, Specification developer2July 30, 2015032api.fda.gov
Metro Mobility Usa LLCMineola, NY, United StatesSpecification developer2January 18, 2022000api.fda.gov
21ST Century Scientific, Inc.Coeur D Alene, ID, United StatesManufacturer1September 3, 2020000api.fda.gov
Amarigo IncLos Angeles, CA, United StatesManufacturer1September 22, 2023000api.fda.gov
Amigo Mobility Intl., Inc.Bridgeport, MI, United StatesManufacturer1December 4, 2009000api.fda.gov
ATZ ManufacturingMarshall, MN, United StatesManufacturer1December 3, 2018000api.fda.gov
Dane TechnologiesMaple Grove, MN, United StatesManufacturer1January 28, 2008000api.fda.gov
Loh Enterprises, LLCClarks Summit, PA, United StatesSpecification developer1March 18, 2021000api.fda.gov
Method Mobility, Inc.Fresno, CA, United StatesManufacturer1May 10, 2023000api.fda.gov
Pride Mobility Products CorporationPontotoc, MS, United StatesManufacturer1May 12, 2022000api.fda.gov
Soul Mobility, IncOconomowoc, WI, United StatesSpecification developer1November 12, 2024000api.fda.gov
Us Shipcell Technology IncMontclair, CA, United StatesSpecification developer1September 22, 2023000api.fda.gov
Deka Research & Development Corp.Manchester, NH, United StatesSpecification developer0000api.fda.gov
Lake Air Products, LLCAppleton, WI, United StatesContract manufacturer0000api.fda.gov
Mobius Mobility LLCManchester, NH, United StatesComplaint file establishment, Manufacturer, Manufacturer for export0000api.fda.gov
Northern Engineering & MFG IncZimmerman, MN, United StatesManufacturer for export0000api.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.