Data / Medical devices / Wheelchair, Mechanical

Wheelchair, Mechanical (IOR): 101 FDA-registered makers in 11 countries

101 establishments in 11 countries are registered with the FDA to make Wheelchair, Mechanical (product code IOR, Class 1, 21 CFR 890.3850). 83 of them have a 510(k) clearance or PMA approval on file and 5 have a recall event. The FDA has issued 468 510(k) clearances under this code, the latest on September 22, 2026, and lists 26 recall events (0 Class I). FDA data exported November 2, 2026.

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Product code

IOR

Device class

1

Regulation

890.3850

Medical specialty

Physical Medicine

Makers by country

Makers of Wheelchair, Mechanical

Registered establishments that manufacture, contract manufacture, remanufacture, reprocess or own the specification of this device, with the 510(k) clearances, PMA approvals and recalls the FDA files under each. Best documented first.

Updated September 22, 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.