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Data / Medical devices / Exerciser, Powered / United States

FDA-registered makers of Exerciser, Powered in the United States: 39 establishments

39 establishments in the United States are registered with the FDA to make Exerciser, Powered (product code BXB). 5 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, Powered
Product code
BXB
Country
United States

Makers of Exerciser, Powered in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Bte TechnologiesHanover, MD, United StatesManufacturer1January 21, 1980000api.fda.gov
Hill LaboratoriesFrazer, PA, United StatesManufacturer1March 31, 1993000api.fda.gov
KLC Services, Inc./ReepLondon, OH, United StatesManufacturer, Remanufacturer1October 5, 1995000api.fda.gov
Swimex SystemsFall River, MA, United StatesManufacturer1January 9, 1995000api.fda.gov
Synthes (USA) Products LLCWest Chester, PA, United StatesComplaint file establishment, Specification developer1January 21, 1983000api.fda.gov
Accelerated Care Plus Corp.Reno, NV, United StatesRepackager or relabeler, Specification developer0010api.fda.gov
Air A Med, LLCFort Myers, FL, United StatesSpecification developer0000api.fda.gov
Aretech,llcSterling, VA, United StatesManufacturer0000api.fda.gov
Bioness Medical, Inc.Valencia, CA, United StatesComplaint file establishment, Manufacturer0000api.fda.gov
Bright Cloud International Corp.Elkton, FL, United StatesManufacturer, Specification developer0000api.fda.gov
Bioventus LLCCordova, TN, United StatesContract manufacturer0000api.fda.gov
Chariot Innovations IncWoodway, TX, United StatesManufacturer0000api.fda.gov
Cirtronics CorporationMilford, NH, United StatesContract manufacturer0000api.fda.gov
CranioMandibular Rehab, Inc.Wheat Ridge, CO, United StatesSpecification developer0000api.fda.gov
Deroyal Industries, Inc.Powell, TN, United StatesComplaint file establishment, Specification developer0000api.fda.gov
E. Bac Si Imports LLCEllensburg, WA, United StatesSpecification developer0000api.fda.gov
ERGO FLEX Technologies LLCConroe, TX, United StatesManufacturer0000api.fda.gov
Full Range Rehab LLCWest Chester, OH, United StatesManufacturer0000api.fda.gov
GK Harmony Enterprises, Inc.Houston, TX, United StatesComplaint file establishment, Manufacturer0000api.fda.gov
H2O For Fitness LLCFort Wayne, IN, United StatesManufacturer0000api.fda.gov
Halley OrthopedicsSouthfield, MI, United StatesManufacturer0000api.fda.gov
Kaiser Medical IncWest Grove, PA, United StatesManufacturer0000api.fda.gov
Kinetec UsaJackson, WI, United StatesSpecification developer0000api.fda.gov
Kinex Medical CompanyWaukesha, WI, United StatesManufacturer0000api.fda.gov
Lite Run IncSaint Paul, MN, United StatesComplaint file establishment, Manufacturer0000api.fda.gov
Motus NovaAtlanta, GA, United StatesManufacturer0000api.fda.gov
Nextstep Robotics Inc.Baltimore, MD, United StatesComplaint file establishment, Manufacturer, Remanufacturer0000api.fda.gov
One Direct HealthMarietta, GA, United StatesManufacturer0000api.fda.gov
Performance Health Systems, LLCNorthbrook, IL, United StatesManufacturer0000api.fda.gov
R & D Batteries, Inc.Burnsville, MN, United StatesManufacturer0000api.fda.gov
REGENERATIVE TECHNOLOGIES CORP dba JUVENTOoltewah, TN, United StatesComplaint file establishment, Manufacturer0000api.fda.gov
Rehabtek LLCLinthicum Heights, MD, United StatesManufacturer0000api.fda.gov
Restorative Therapies Inc.Nottingham, MD, United StatesManufacturer0000api.fda.gov
Sport Medical Technology IncShirley, NY, United StatesManufacturer0000api.fda.gov
Titin KM Biomedical Corp.Bozeman, MT, United StatesComplaint file establishment, Manufacturer, Remanufacturer0000api.fda.gov
The Furniss Corporation LtdMount Sterling, OH, United StatesManufacturer0000api.fda.gov
Vibetech Enterprises, LLCSheboygan, WI, United StatesManufacturer0000api.fda.gov
Xeras Medical TechnologiesSan Antonio, TX, United StatesSpecification developer0000api.fda.gov
Zona Health, Inc.Montgomery, AL, United StatesComplaint file establishment, Manufacturer, Manufacturer for export0000api.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.