Data / Medical devices / Stretcher, Wheeled / United States

FDA-registered makers of Stretcher, Wheeled in the United States: 23 establishments

Name: FDA-registered makers of Stretcher, Wheeled in the United States
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

23 establishments in the United States are registered with the FDA to make Stretcher, Wheeled (product code FPO). 1 has a 510(k) clearance or PMA approval on file and 4 have a recall event. FDA data exported November 2, 2026.

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Device: Stretcher, Wheeled
Product code: FPO
Country: United States

Makers of Stretcher, Wheeled in the United States

Maker	Location	Role	510(k) clearances	Latest clearance	Recall events	Source
Stryker Medical	Portage, MI, United States	Complaint file establishment, Manufacturer, Specification developer	1	December 20, 2011	19	api.fda.gov
21ST Century Scientific, Inc.	Coeur D Alene, ID, United States	Manufacturer	0		0	api.fda.gov
Bound Tree Medical, LLC	Grand Prairie, TX, United States	Manufacturer	0		0	api.fda.gov
Caf Medical Solutions Inc	Hockley, TX, United States	Manufacturer	0		0	api.fda.gov
Diacor, Inc.	Mount Pleasant, UT, United States	Manufacturer	0		0	api.fda.gov
Electro-Connect, Inc.	Milwaukee, WI, United States	Complaint file establishment, Contract manufacturer, Manufacturer	0		0	api.fda.gov
Faretec, Inc.	Painesville, OH, United States	Manufacturer	0		0	api.fda.gov
Ferno-Washington, Inc.	Wilmington, OH, United States	Complaint file establishment, Manufacturer, Specification developer	0		11	api.fda.gov
GF Health Products, Inc	Atlanta, GA, United States	Manufacturer	0		0	api.fda.gov
GF Health Products, Inc.	Fond du Lac, WI, United States	Manufacturer	0		0	api.fda.gov
Healthline Medical Products	Winter Garden, FL, United States	Manufacturer	0		0	api.fda.gov
Hill-Rom, Inc.	Batesville, IN, United States	Complaint file establishment, Manufacturer, Repackager or relabeler, Specification developer	0		1	api.fda.gov
Hosmed Inc.	Doral, FL, United States	Manufacturer, Repackager or relabeler	0		0	api.fda.gov
Haywood Vocational Opportunities Inc.	Waynesville, NC, United States	Manufacturer	0		0	api.fda.gov
Jac Custom Pouches	Dowagiac, MI, United States	Contract manufacturer	0		0	api.fda.gov
Klyo Medical Systems Inc	Doral, FL, United States	Manufacturer, Repackager or relabeler	0		0	api.fda.gov
Mac Medical	Millstadt, IL, United States	Contract manufacturer, Manufacturer, Remanufacturer	0		0	api.fda.gov
Mirion Technologies (capintec), Inc	Florham Park, NJ, United States	Manufacturer	0		0	api.fda.gov
MJM International Corporation	Edinburg, TX, United States	Manufacturer	0		0	api.fda.gov
Mor-Medical International	Pharr, TX, United States	Manufacturer	0		0	api.fda.gov
Pedigo Products, Inc.	Vancouver, WA, United States	Manufacturer	0		0	api.fda.gov
Sechrist Industries, Inc.	Anaheim, CA, United States	Manufacturer	0		3	api.fda.gov
Setmark Inc.	Cheyenne, WY, United States	Specification developer	0		0	api.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.