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Data / Medical devices / Stretcher, Hand-Carried / United States

FDA-registered makers of Stretcher, Hand-Carried in the United States: 24 establishments

24 establishments in the United States are registered with the FDA to make Stretcher, Hand-Carried (product code FPP). 0 have a 510(k) clearance or PMA approval on file and 1 has a recall event. FDA data exported November 2, 2026.

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Device
Stretcher, Hand-Carried
Product code
FPP
Country
United States

Makers of Stretcher, Hand-Carried in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
3FDM, Inc.Largo, FL, United StatesContract manufacturer0000api.fda.gov
Advanced Instrumentations, Inc.Miami, FL, United StatesManufacturer0000api.fda.gov
Aspen Surgical Products, Inc.Caledonia, MI, United StatesComplaint file establishment, Specification developer0000api.fda.gov
Allied Medical LLCEarth City, MO, United StatesManufacturer, Repackager or relabeler, Specification developer0000api.fda.gov
BINDER LIFT Inc.DBA PHASEBigfork, MT, United StatesSpecification developer0000api.fda.gov
Casco Manufacturing Solutions, Inc.Cincinnati, OH, United StatesManufacturer0000api.fda.gov
Domico Med-Device, LLCFenton, MI, United StatesManufacturer0000api.fda.gov
Emergency Products & Research, Inc.Kent, OH, United StatesManufacturer0000api.fda.gov
Ferno-Washington, Inc.Wilmington, OH, United StatesComplaint file establishment, Manufacturer, Repackager or relabeler, Specification developer0000api.fda.gov
Formed Plastics, Inc.Carle Place, NY, United StatesManufacturer0000api.fda.gov
Innovative Products Unlimited, Inc.Niles, MI, United StatesManufacturer0000api.fda.gov
Junkin Safety Appliance Co., Inc.Louisville, KY, United StatesManufacturer0000api.fda.gov
Lifesaving Systems, LLCApollo Beach, FL, United StatesManufacturer0000api.fda.gov
Little Rapids CorporationGreen Bay, WI, United StatesSpecification developer0000api.fda.gov
North American Rescue, LLC.Greer, SC, United StatesManufacturer, Repackager or relabeler, Specification developer0000api.fda.gov
NYOrthoBrooklyn, NY, United StatesManufacturer0000api.fda.gov
RED MEDICAL CORPORATION dba Med Tech Sweden Inc (Unit # 4, 3 and Office)Geneseo, IL, United StatesManufacturer0000api.fda.gov
Stryker MedicalPortage, MI, United StatesComplaint file establishment, Manufacturer0040api.fda.gov
SunmedicaRedding, CA, United StatesManufacturer0000api.fda.gov
Tacmed Solutions, LLCAnderson, SC, United StatesSpecification developer0000api.fda.gov
Taylor Healthcare Products, IncSpring, TX, United StatesSpecification developer0000api.fda.gov
Tri-Tech Forensics, Inc.Leland, NC, United StatesManufacturer, Specification developer0000api.fda.gov
Tenacious Holdings IncSaint Paul, MN, United StatesSpecification developer0000api.fda.gov
Xodus Medical, Inc.New Kensington, PA, 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.