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Data / Medical devices / Cart, Emergency, Cardiopulmonary (Excluding Equipment) / United States

FDA-registered makers of Cart, Emergency, Cardiopulmonary (Excluding Equipment) in the United States: 33 establishments

33 establishments in the United States are registered with the FDA to make Cart, Emergency, Cardiopulmonary (Excluding Equipment) (product code BZN). 0 have a 510(k) clearance or PMA approval on file and 1 has a recall event. FDA data exported November 3, 2026.

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Device
Cart, Emergency, Cardiopulmonary (Excluding Equipment)
Product code
BZN
Country
United States

Makers of Cart, Emergency, Cardiopulmonary (Excluding Equipment) in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Afc Industries Pa, IncBerwick, PA, United StatesContract manufacturer0000api.fda.gov
Arthrex, Inc.Naples, FL, United StatesSpecification developer0000api.fda.gov
Arthrex, Inc.Ave Maria, FL, United StatesContract manufacturer, Contract sterilizer0000api.fda.gov
BiosealPlacentia, CA, United StatesContract manufacturer, Manufacturer, Repackager or relabeler0000api.fda.gov
Capsa HealthcareCanal Winchester, OH, United StatesComplaint file establishment, Manufacturer0000api.fda.gov
Cardinal Scale MFG. Co.Webb City, MO, United StatesManufacturer0000api.fda.gov
Claflin Service CompanyWarwick, RI, United StatesComplaint file establishment, Manufacturer0000api.fda.gov
ClearPoint Neuro Inc.Carlsbad, CA, United StatesManufacturer0000api.fda.gov
Depuy Spine, Inc.Raynham, MA, United StatesSpecification developer0000api.fda.gov
DePuy Synthes West Palm BeachWest Palm Beach, FL, United StatesManufacturer0000api.fda.gov
Doner Industries, Inc.Rogers, AR, United StatesSpecification developer0000api.fda.gov
Galvanize TherapeuticsRedwood City, CA, United StatesComplaint file establishment, Manufacturer0000api.fda.gov
Innovative Products Unlimited, Inc.Niles, MI, United StatesManufacturer0000api.fda.gov
Intermetro Industries CorpWilkes Barre, PA, United StatesSpecification developer0000api.fda.gov
Iroquois Industrial Group, LLC d.b.a T & D METAL PRODUCTSWatseka, IL, United StatesManufacturer0000api.fda.gov
Luxor Workspaces LLC, A Subsidiary Of Ebsco Industries, Inc.Waukegan, IL, United StatesSpecification developer0000api.fda.gov
Mada Medical Products, Inc.Carlstadt, NJ, United StatesManufacturer, Repackager or relabeler0000api.fda.gov
MJM International CorporationEdinburg, TX, United StatesManufacturer0000api.fda.gov
Modo IncHillsboro, OR, United StatesContract manufacturer0000api.fda.gov
Mor-Medical InternationalPharr, TX, United StatesManufacturer0000api.fda.gov
Medtronic VascularSanta Rosa, CA, United StatesSpecification developer0000api.fda.gov
Merit Medical Systems, Inc.Aliso Viejo, CA, United StatesSpecification developer0000api.fda.gov
Millstone Medical Outsourcing LLCOlive Branch, MS, United StatesContract manufacturer0000api.fda.gov
Modo, Inc.McMinnville, OR, United StatesContract manufacturer0000api.fda.gov
Nova Ortho-Med, Inc.North Aurora, IL, United StatesSpecification developer0000api.fda.gov
Northgate Technologies Inc.Elgin, IL, United StatesComplaint file establishment, Repackager or relabeler, Specification developer0000api.fda.gov
PENTAX of America, Inc.Montvale, NJ, United StatesComplaint file establishment, Manufacturer, Specification developer0000api.fda.gov
Re:build Tekna, LLCKalamazoo, MI, United StatesContract manufacturer0000api.fda.gov
Santa Barbara Imaging SystemsGoleta, CA, United StatesManufacturer, Repackager or relabeler, Specification developer0000api.fda.gov
Stryker EndoscopySan Jose, CA, United StatesSpecification developer0020api.fda.gov
The Harloff Company, Inc.Colorado Springs, CO, United StatesManufacturer0000api.fda.gov
TOUCHPOINT MEDICAL, Inc.Odessa, FL, United StatesContract manufacturer, Manufacturer0000api.fda.gov
Zoll Medical CorporationChelmsford, MA, United StatesComplaint file establishment, Manufacturer0000api.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.