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Data / Medical devices / Cane / United States

FDA-registered makers of Cane in the United States: 14 establishments

14 establishments in the United States are registered with the FDA to make Cane (product code IPS). 0 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.

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Device
Cane
Product code
IPS
Country
United States

Makers of Cane in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Aligned AS Designed, LLCPasadena, CA, United StatesManufacturer0000api.fda.gov
ASP Global, LLCAustell, GA, United StatesSpecification developer0000api.fda.gov
Fashionable, Inc.Largo, FL, United StatesSpecification developer0000api.fda.gov
Harvy Surgical Supply Corp.Flushing, NY, United StatesRepackager or relabeler, Specification developer0000api.fda.gov
In-Step Mobility Products CorporationSkokie, IL, United StatesManufacturer0000api.fda.gov
J & D Tech IncNesconset, NY, United StatesComplaint file establishment, Repackager or relabeler, Specification developer0000api.fda.gov
MEDLINE INDUSTRIES, LP - NorthfieldNorthfield, IL, United StatesSpecification developer0000api.fda.gov
Merchsource LLCIrvine, CA, United StatesSpecification developer0000api.fda.gov
Medegen Medical ProductsGallaway, TN, United StatesSpecification developer0000api.fda.gov
P.C.P. ChampionRipley, OH, United StatesManufacturer, Repackager or relabeler0000api.fda.gov
Secured Ortho Manufacturing Of America, LLCDeer Park, NY, United StatesManufacturer, Specification developer0000api.fda.gov
Span Link International LLCDeer Park, NY, United StatesSpecification developer0000api.fda.gov
Transparent Supply Solutions Ltd.Dover, DE, United StatesSpecification developer0000api.fda.gov
Telo LLCMinneapolis, MN, United StatesManufacturer0000api.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.