Data / Medical devices / Electromyograph, Diagnostic / United States

FDA-registered makers of Electromyograph, Diagnostic in the United States: 35 establishments

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

35 establishments in the United States are registered with the FDA to make Electromyograph, Diagnostic (product code IKN). 7 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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Device: Electromyograph, Diagnostic
Product code: IKN
Country: United States

Makers of Electromyograph, Diagnostic in the United States

Maker	Location	Role	510(k) clearances	Latest clearance	Source
Medtronic Xomed, Inc.	Jacksonville, FL, United States	Manufacturer	2	January 6, 2003	api.fda.gov
Cadwell Industries, Inc.	Kennewick, WA, United States	Manufacturer	1	March 1, 2017	api.fda.gov
Integrated Biomedical Corp.	Las Vegas, NV, United States	Manufacturer	1	December 27, 1983	api.fda.gov
Nihon Kohden America, Inc.	Irvine, CA, United States	Complaint file establishment, Manufacturer	1	June 28, 2001	api.fda.gov
Natus Neurology Incorporated	Middleton, WI, United States	Manufacturer, Specification developer	1	December 19, 2017	api.fda.gov
SRS Medical	Chelmsford, MA, United States	Manufacturer	1	August 16, 2007	api.fda.gov
Uroval Inc/Folkerts	Manhattan, KS, United States	Manufacturer	1	September 11, 2009	api.fda.gov
Alphatec Spine, Inc.	Carlsbad, CA, United States	Manufacturer, Specification developer	0		api.fda.gov
ARCH Medical Solutions - Memphis	Bartlett, TN, United States	Contract manufacturer	0		api.fda.gov
ARCH Medical Solutions - Memphis	Lexington, TN, United States	Contract manufacturer	0		api.fda.gov
ARCH Medical Solutions - Olive Branch	Olive Branch, MS, United States	Contract manufacturer	0		api.fda.gov
ARCH Medical Solutions - Seabrook	Seabrook, NH, United States	Contract manufacturer	0		api.fda.gov
Alphatec Spine, Inc.	Memphis, TN, United States	Manufacturer	0		api.fda.gov
Avalign Instruments & Implants	Fort Wayne, IN, United States	Contract manufacturer	0		api.fda.gov
Culver Tool & Engineering	Plymouth, IN, United States	Contract manufacturer	0		api.fda.gov
Cardinal Health	Wabasha, MN, United States	Contract manufacturer	0		api.fda.gov
Ducommun LaBarge Technologies	Appleton, WI, United States	Contract manufacturer	0		api.fda.gov
Engineered Medical Systems, LLC	Bartlett, TN, United States	Contract manufacturer	0		api.fda.gov
Ferry Machine Corporation	Oakland, NJ, United States	Contract manufacturer	0		api.fda.gov
Ferry Machine Corporation	Little Ferry, NJ, United States	Contract manufacturer	0		api.fda.gov
Globus Medical, Inc.	Memphis, TN, United States	Manufacturer	0		api.fda.gov
Insert Molding Solutions, Inc.	Cumming, GA, United States	Contract manufacturer	0		api.fda.gov
Katecho LLC	Des Moines, IA, United States	Contract manufacturer	0		api.fda.gov
Life Science Outsourcing, Inc.	Brea, CA, United States	Contract manufacturer	0		api.fda.gov
Mackay Manufacturing, Inc.	Spokane Valley, WA, United States	Contract manufacturer	0		api.fda.gov
Nortech Systems, Inc.	Milaca, MN, United States	Contract manufacturer	0		api.fda.gov
Nuvasive, Inc.	Guaynabo, PR, United States	Manufacturer	0		api.fda.gov
Nuvasive, Inc.	San Diego, CA, United States	Manufacturer	0		api.fda.gov
Onyx Healthcare Usa, Inc.	Orange, CA, United States	Manufacturer	0		api.fda.gov
Remington Medical, Inc.	Alpharetta, GA, United States	Contract manufacturer	0		api.fda.gov
RMS Co.	Minneapolis, MN, United States	Contract manufacturer	0		api.fda.gov
Remington Medical, Inc.	Alpharetta, GA, United States	Contract manufacturer	0		api.fda.gov
Structure Medical, LLC.	Naples, FL, United States	Contract manufacturer	0		api.fda.gov
Spartronics Watertown LLC	Watertown, SD, United States	Contract manufacturer	0		api.fda.gov
Turner Medical Inc.	Athens, AL, United States	Contract manufacturer	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.