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
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Bte Technologies | Hanover, MD, United States | Manufacturer | 1 | January 21, 1980 | 0 | 0 | 0 | api.fda.gov |
| Hill Laboratories | Frazer, PA, United States | Manufacturer | 1 | March 31, 1993 | 0 | 0 | 0 | api.fda.gov |
| KLC Services, Inc./Reep | London, OH, United States | Manufacturer, Remanufacturer | 1 | October 5, 1995 | 0 | 0 | 0 | api.fda.gov |
| Swimex Systems | Fall River, MA, United States | Manufacturer | 1 | January 9, 1995 | 0 | 0 | 0 | api.fda.gov |
| Synthes (USA) Products LLC | West Chester, PA, United States | Complaint file establishment, Specification developer | 1 | January 21, 1983 | 0 | 0 | 0 | api.fda.gov |
| Accelerated Care Plus Corp. | Reno, NV, United States | Repackager or relabeler, Specification developer | 0 | 0 | 1 | 0 | api.fda.gov | |
| Air A Med, LLC | Fort Myers, FL, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Aretech,llc | Sterling, VA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Bioness Medical, Inc. | Valencia, CA, United States | Complaint file establishment, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Bright Cloud International Corp. | Elkton, FL, United States | Manufacturer, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Bioventus LLC | Cordova, TN, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Chariot Innovations Inc | Woodway, TX, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Cirtronics Corporation | Milford, NH, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| CranioMandibular Rehab, Inc. | Wheat Ridge, CO, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Deroyal Industries, Inc. | Powell, TN, United States | Complaint file establishment, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| E. Bac Si Imports LLC | Ellensburg, WA, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| ERGO FLEX Technologies LLC | Conroe, TX, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Full Range Rehab LLC | West Chester, OH, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| GK Harmony Enterprises, Inc. | Houston, TX, United States | Complaint file establishment, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| H2O For Fitness LLC | Fort Wayne, IN, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Halley Orthopedics | Southfield, MI, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Kaiser Medical Inc | West Grove, PA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Kinetec Usa | Jackson, WI, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Kinex Medical Company | Waukesha, WI, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Lite Run Inc | Saint Paul, MN, United States | Complaint file establishment, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Motus Nova | Atlanta, GA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Nextstep Robotics Inc. | Baltimore, MD, United States | Complaint file establishment, Manufacturer, Remanufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| One Direct Health | Marietta, GA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Performance Health Systems, LLC | Northbrook, IL, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| R & D Batteries, Inc. | Burnsville, MN, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| REGENERATIVE TECHNOLOGIES CORP dba JUVENT | Ooltewah, TN, United States | Complaint file establishment, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Rehabtek LLC | Linthicum Heights, MD, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Restorative Therapies Inc. | Nottingham, MD, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Sport Medical Technology Inc | Shirley, NY, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Titin KM Biomedical Corp. | Bozeman, MT, United States | Complaint file establishment, Manufacturer, Remanufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| The Furniss Corporation Ltd | Mount Sterling, OH, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Vibetech Enterprises, LLC | Sheboygan, WI, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Xeras Medical Technologies | San Antonio, TX, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Zona Health, Inc. | Montgomery, AL, United States | Complaint file establishment, Manufacturer, Manufacturer for export | 0 | 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.