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Data / Medical devices / Crutch / United States

FDA-registered makers of Crutch in the United States: 23 establishments

23 establishments in the United States are registered with the FDA to make Crutch (product code IPR). 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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Get makers of this device in the United StatesWatch these makers
Device
Crutch
Product code
IPR
Country
United States

Makers of Crutch 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
Djo, LLCCarlsbad, CA, United StatesSpecification developer0000api.fda.gov
Ergoactives, LLCMiami, FL, United StatesSpecification developer0000api.fda.gov
Harvy Surgical Supply Corp.Flushing, NY, United StatesRepackager or relabeler, Specification developer0000api.fda.gov
Iwalkfree, Inc.Long Beach, CA, United StatesManufacturer, Specification developer0000api.fda.gov
J & D Tech IncNesconset, NY, United StatesComplaint file establishment, Repackager or relabeler, Specification developer0000api.fda.gov
Manamed LLCDenton, TX, United StatesSpecification developer0000api.fda.gov
MEDLINE INDUSTRIES, LP - NorthfieldNorthfield, IL, United StatesSpecification developer0000api.fda.gov
Medegen Medical ProductsGallaway, TN, United StatesSpecification developer0000api.fda.gov
Mobi Acquisition CompanySaint Louis Park, MN, United StatesSpecification developer0000api.fda.gov
Onlycare IncDenver, CO, United StatesManufacturer0000api.fda.gov
P.C.P. ChampionRipley, OH, United StatesManufacturer, Repackager or relabeler0000api.fda.gov
Peak Degrees LLCSouthlake, TX, United StatesSpecification developer0000api.fda.gov
Secured Ortho Manufacturing Of America, LLCDeer Park, NY, United StatesManufacturer, Specification developer0000api.fda.gov
Smith & Nephew, Inc.Memphis, TN, United StatesManufacturer0000api.fda.gov
Span Link International LLCDeer Park, NY, United StatesSpecification developer0000api.fda.gov
Smith & Nephew, Inc.Memphis, TN, United StatesManufacturer0000api.fda.gov
Smith & Nephew, Inc.Memphis, TN, United StatesManufacturer0000api.fda.gov
Top Shelf Manufacturing, LLCTracy, CA, United StatesManufacturer0000api.fda.gov
Transparent Supply Solutions Ltd.Dover, DE, United StatesSpecification developer0000api.fda.gov
Unite Medical, LLCLithia Springs, GA, United StatesSpecification developer0000api.fda.gov
United Surgical LLCLaotto, IN, United StatesRepackager or relabeler, Specification developer0000api.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.