Data / Medical devices / Interactive Rehabilitation Exercise Device, Prescription Use / United States

FDA-registered makers of Interactive Rehabilitation Exercise Device, Prescription Use in the United States: 21 establishments

Name: FDA-registered makers of Interactive Rehabilitation Exercise Device, Prescription Use in the United States
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

21 establishments in the United States are registered with the FDA to make Interactive Rehabilitation Exercise Device, Prescription Use (product code QKC). 0 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 3, 2026.

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Device: Interactive Rehabilitation Exercise Device, Prescription Use
Product code: QKC
Country: United States

Makers of Interactive Rehabilitation Exercise Device, Prescription Use in the United States

Maker	Location	Role	Source
Amp Health Inc	Aspen, CO, United States	Complaint file establishment, Manufacturer	api.fda.gov
Axolohealth	Charlotte, NC, United States	Manufacturer	api.fda.gov
Band Connect	Cincinnati, OH, United States	Specification developer	api.fda.gov
Bioness Medical, Inc.	Valencia, CA, United States	Complaint file establishment, Manufacturer	api.fda.gov
Curveassure Inc.	Towson, MD, United States	Complaint file establishment, Manufacturer	api.fda.gov
Exer Labs, Inc.	Denver, CO, United States	Manufacturer	api.fda.gov
Kaia Health Software Inc	New York, NY, United States	Specification developer	api.fda.gov
Karuna Labs	Ione, CA, United States	Reprocessor	api.fda.gov
Lainahealth	Dublin, OH, United States	Manufacturer	api.fda.gov
M.R.S. Health, Inc.	Lenox, MI, United States	Complaint file establishment, Manufacturer	api.fda.gov
Neurotechr3 Inc.	Warren, NJ, United States	Manufacturer	api.fda.gov
NeckCare Enterprises, Inc	Minneapolis, MN, United States	Complaint file establishment, Contract manufacturer	api.fda.gov
NeuroX USA Inc	Raleigh, NC, United States	Contract manufacturer, Repackager or relabeler	api.fda.gov
OpenMotion AI, Inc.	Dripping Springs, TX, United States	Manufacturer	api.fda.gov
Percix Corp	Portland, OR, United States	Manufacturer	api.fda.gov
STROLLL, Inc.	Cleveland, OH, United States	Manufacturer	api.fda.gov
Torque3	Centerville, UT, United States	Manufacturer	api.fda.gov
Verity Technologies	Elmhurst, IL, United States	Complaint file establishment, Manufacturer	api.fda.gov
Virtusense	Peoria, IL, United States	Manufacturer	api.fda.gov
Xperience Robotics Inc. D/B/A Ugen	Cuyahoga Falls, OH, United States	Manufacturer, Specification developer	api.fda.gov
Yoursteps Health, Inc.	Eagan, MN, United States	Specification developer	api.fda.gov

Updated November 3, 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.