Data / Medical devices / Cable, Electrode / United States

FDA-registered makers of Cable, Electrode in the United States: 62 establishments

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

62 establishments in the United States are registered with the FDA to make Cable, Electrode (product code IKD). 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: Cable, Electrode
Product code: IKD
Country: United States

Makers of Cable, Electrode in the United States

Maker	Location	Role	510(k) clearances	Latest clearance	Recall events	Class I	Source
Oscor Inc.	Palm Harbor, FL, United States	Complaint file establishment, Manufacturer	1	June 7, 2007	1	1	api.fda.gov
Access Point Technologies, Ep Inc.	Rogers, MN, United States	Complaint file establishment, Manufacturer	0		0	0	api.fda.gov
Ad-Tech Medical Instrument Corp.	Oak Creek, WI, United States	Manufacturer	0		2	0	api.fda.gov
Alphatec Spine, Inc.	Carlsbad, CA, United States	Manufacturer, Specification developer	0		0	0	api.fda.gov
Alto Development Corp.	Farmingdale, NJ, United States	Manufacturer	0		0	0	api.fda.gov
Atrility Medical, Inc.	Madison, WI, United States	Specification developer	0		0	0	api.fda.gov
Avazzia, Inc.	Dallas, TX, United States	Manufacturer	0		0	0	api.fda.gov
Alphatec Spine, Inc.	Memphis, TN, United States	Manufacturer	0		0	0	api.fda.gov
Braemar Manufacturing, LLC	Eagan, MN, United States	Complaint file establishment, Manufacturer	0		0	0	api.fda.gov
Boston Scientific Corporation	Coventry, RI, United States	Manufacturer	0		0	0	api.fda.gov
Boston Scientific Corporation	Waltham, MA, United States	Specification developer	0		0	0	api.fda.gov
Braemar Manufacturing, LLC	San Diego, CA, United States	Specification developer	0		0	0	api.fda.gov
Cadwell Industries, Inc.	Kennewick, WA, United States	Manufacturer, Specification developer	0		0	0	api.fda.gov
Cardinal Health	Riverview, FL, United States	Manufacturer, Reprocessor	0		0	0	api.fda.gov
Cardionet, LLC	Phoenix, AZ, United States	Complaint file establishment, Contract manufacturer	0		0	0	api.fda.gov
Cardionet, LLC	Linwood, PA, United States	Complaint file establishment, Contract manufacturer	0		0	0	api.fda.gov
CEA Medical Manufacturing, Inc.	Colorado Springs, CO, United States	Contract manufacturer	0		0	0	api.fda.gov
CIRCA Scientific, Inc.	Englewood, CO, United States	Manufacturer, Specification developer	0		0	0	api.fda.gov
Clearpath Medical, LLC	Tustin, CA, United States	Contract manufacturer	0		0	0	api.fda.gov
Conmed Corporation	Utica, NY, United States	Manufacturer	0		0	0	api.fda.gov
Cardinal Health	Hazelwood, MO, United States	Specification developer	0		0	0	api.fda.gov
Conmed Corporation	Westborough, MA, United States	Specification developer	0		0	0	api.fda.gov
Cortex, Inc.	Santa Clara, CA, United States	Specification developer	0		0	0	api.fda.gov
Djo, LLC	Carlsbad, CA, United States	Specification developer	0		0	0	api.fda.gov
Datex-Ohmeda, Inc.	Wauwatosa, WI, United States	Specification developer	0		0	0	api.fda.gov
Datex-Ohmeda, Inc.	Waukesha, WI, United States	Specification developer	0		0	0	api.fda.gov
GE Medical Systems Information Technologies, Inc.	Waukesha, WI, United States	Specification developer	0		0	0	api.fda.gov
GE Medical Systems Information Technologies, Inc.	Wauwatosa, WI, United States	Specification developer	0		0	0	api.fda.gov
Innovative Health, LLC.	Scottsdale, AZ, United States	Reprocessor	0		0	0	api.fda.gov
Intelligent Hearing Systems Corp.	Miami, FL, United States	Manufacturer, Specification developer	0		0	0	api.fda.gov
Irvine Biomedical. Inc.	Irvine, CA, United States	Manufacturer, Manufacturer for export, Specification developer	0		0	0	api.fda.gov
LifeSync Corporation	Coral Springs, FL, United States	Complaint file establishment, Specification developer	0		0	0	api.fda.gov
Med-Dyne	Louisville, KY, United States	Manufacturer	0		0	0	api.fda.gov
Med-Linket Corp	Alhambra, CA, United States	Manufacturer	0		0	0	api.fda.gov
MEDLINE INDUSTRIES, LP - Northfield	Northfield, IL, United States	Complaint file establishment, Specification developer	0		0	0	api.fda.gov
Merit Cables Inc.	Santa Ana, CA, United States	Manufacturer	0		0	0	api.fda.gov
Medline ReNewal	Redmond, OR, United States	Reprocessor	0		0	0	api.fda.gov
Neurovision Medical Products, Inc.	Ventura, CA, United States	Manufacturer	0		0	0	api.fda.gov
Nuvasive, Inc.	Guaynabo, PR, United States	Manufacturer	0		0	0	api.fda.gov
Nuvasive, Inc.	San Diego, CA, United States	Complaint file establishment, Manufacturer, Specification developer	0		0	0	api.fda.gov
Natus Neurology Incorporated	Middleton, WI, United States	Specification developer	0		0	0	api.fda.gov
Neurotron Inc	Aurora, CO, United States	Manufacturer	0		0	0	api.fda.gov
Nypro Inc (Maple Grove)	Maple Grove, MN, United States	Contract manufacturer	0		0	0	api.fda.gov
P1 Technologies, Inc.	Cave Spring, VA, United States	Contract manufacturer	0		0	0	api.fda.gov
Peter Schiff Enterprise	Cookeville, TN, United States	Manufacturer	0		0	0	api.fda.gov
PMT Corp.	Chanhassen, MN, United States	Manufacturer, Remanufacturer, Repackager or relabeler, Specification developer	0		0	0	api.fda.gov
Philips North America LLC	Cambridge, MA, United States	Specification developer	0		0	0	api.fda.gov
Philips North America LLC	Andover, MA, United States	Specification developer	0		0	0	api.fda.gov
Philips North America LLC	Bothell, WA, United States	Specification developer	0		0	0	api.fda.gov
Philips North America LLC	Woodinville, WA, United States	Specification developer	0		0	0	api.fda.gov
Renu Medical, Inc.	Everett, WA, United States	Complaint file establishment, Repackager or relabeler, Reprocessor	0		0	0	api.fda.gov
Rhythmlink International, LLC	Columbia, SC, United States	Manufacturer, Repackager or relabeler, Specification developer	0		0	0	api.fda.gov
Remington Medical, Inc.	Alpharetta, GA, United States	Contract manufacturer	0		0	0	api.fda.gov
St. Jude Medical	Roseville, MN, United States	Manufacturer, Manufacturer for export	0		0	0	api.fda.gov
St. Jude Medical, Atrial Fibrillation Division, Inc.	Saint Paul, MN, United States	Specification developer	0		0	0	api.fda.gov
St. Jude Medical, Atrial Fibrillation Division, Inc.	Minnetonka, MN, United States	Manufacturer, Manufacturer for export, Specification developer	0		1	0	api.fda.gov
St. Jude Medical, Cardiology Division, Inc.	Plymouth, MN, United States	Complaint file establishment, Manufacturer, Specification developer	0		0	0	api.fda.gov
Stryker Sustainability Solutions	Tempe, AZ, United States	Specification developer	0		1	0	api.fda.gov
Technical Services For Electronics, Inc.	Jackson, MN, United States	Contract manufacturer	0		0	0	api.fda.gov
The Electrode Store	Buckley, WA, United States	Manufacturer	0		0	0	api.fda.gov
Uroval Inc/Folkerts	Manhattan, KS, United States	Manufacturer	0		0	0	api.fda.gov
Zien Medical Technologies LLC	Salt Lake City, UT, United States	Contract manufacturer	0		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.