Data / Medical devices / Exerciser, Measuring / United States

FDA-registered makers of Exerciser, Measuring in the United States: 23 establishments

Name: FDA-registered makers of Exerciser, Measuring 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 Exerciser, Measuring (product code ISD). 3 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: Exerciser, Measuring
Product code: ISD
Country: United States

Makers of Exerciser, Measuring in the United States

Maker	Location	Role	510(k) clearances	Latest clearance	Recall events	Source
ActiGraph L.L.C.	Pensacola, FL, United States	Manufacturer, Repackager or relabeler, Specification developer	1	July 24, 2008	0	api.fda.gov
Bte Technologies	Hanover, MD, United States	Manufacturer	1	June 20, 1994	1	api.fda.gov
Welch Allyn, Inc.	Skaneateles Falls, NY, United States	Specification developer	1	April 27, 2006	0	api.fda.gov
APDM Wearable Technologies, Inc.	Portland, OR, United States	Manufacturer	0		0	api.fda.gov
BAL Inc	Sunnyvale, CA, United States	Specification developer	0		0	api.fda.gov
Bertec Corp.	Columbus, OH, United States	Manufacturer	0		0	api.fda.gov
Bioness Medical, Inc.	Valencia, CA, United States	Complaint file establishment, Manufacturer	0		0	api.fda.gov
Biosensics	Newton, MA, United States	Complaint file establishment, Manufacturer	0		0	api.fda.gov
Bright Cloud International Corp.	Elkton, FL, United States	Manufacturer, Specification developer	0		0	api.fda.gov
Exer Labs, Inc.	Denver, CO, United States	Manufacturer	0		0	api.fda.gov
Foresite Healthcare, LLC	Maryland Heights, MO, United States	Manufacturer	0		0	api.fda.gov
Janzen And Janzen Chiropractic Corporation	Oklahoma City, OK, United States	Manufacturer	0		0	api.fda.gov
Katecho LLC	Des Moines, IA, United States	Contract manufacturer	0		0	api.fda.gov
Medthera Inc.	Waconia, MN, United States	Specification developer	0		0	api.fda.gov
Mirac, LLC	Lynchburg, OH, United States	Contract manufacturer	0		0	api.fda.gov
Neuro Rehab VR	Fort Worth, TX, United States	Manufacturer	0		0	api.fda.gov
Plethy	Santa Clara, CA, United States	Manufacturer	0		0	api.fda.gov
Pro2health, Inc.	Cleveland, OH, United States	Manufacturer	0		0	api.fda.gov
Prove Labs inc	Brooklyn, NY, United States	Manufacturer	0		0	api.fda.gov
Rune Labs Inc.	San Francisco, CA, United States	Manufacturer	0		0	api.fda.gov
Seniorlife Technologies Inc	Bellevue, WA, United States	Manufacturer	0		0	api.fda.gov
Stridelink Inc.	Atlanta, GA, United States	Manufacturer	0		0	api.fda.gov
SWORD Health, Inc	Salt Lake City, UT, United States	Manufacturer	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.