Data / Medical devices / Treadmill, Powered
Treadmill, Powered (IOL): 22 FDA-registered makers in 8 countries
22 establishments in 8 countries are registered with the FDA to make Treadmill, Powered (product code IOL, Class 1, 21 CFR 890.5380). 0 of them have a 510(k) clearance or PMA approval on file and 1 has a recall event. The FDA has issued 43 510(k) clearances under this code, the latest on September 6, 1995, and lists 7 recall events (0 Class I). FDA data exported November 2, 2026.
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- Product code
- IOL
- Device class
- 1
- Regulation
- 890.5380
- Medical specialty
- Physical Medicine
Makers by country
| Country | Makers |
|---|---|
| United States | 7 |
| China | 5 |
| India | 2 |
| Germany | 2 |
| South Korea | 2 |
| Netherlands | 2 |
| Taiwan | 1 |
| Israel | 1 |
Makers of Treadmill, Powered
Registered establishments that manufacture, contract manufacture, remanufacture, reprocess or own the specification of this device, with the 510(k) clearances, PMA approvals and recalls the FDA files under each. Best documented first.
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Advanced Mechanical Technology Inc | Watertown, MA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Apothecaries Sundries MFG Pvt Ltd | GURUGRAM Haryana, India | Manufacturer, Repackager or relabeler | 0 | 0 | 0 | 0 | api.fda.gov | |
| Body Charger Fitness Int'l Corp(gee Hoo Fitec Corp) | Yuanlin City Changhua, Taiwan | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Edan Instruments, Inc. | Shenzhen Guangdong, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Ekso Bionics | San Rafael, CA, United States | Complaint file establishment, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Full Vision, Inc. | Newton, KS, United States | Manufacturer | 0 | 0 | 2 | 0 | api.fda.gov | |
| Fourier Intelligence Inc. | Shanghai, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Goldengait Ltd. | Bnei Brak Central, Israel | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Greens Surgicals Private Limited | Vadodara Gujarat, India | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| H/P/Cosmos Sports & Medical GMBH | NUSSDORF BEI TRAUNSTEIN Bavaria, Germany | Contract manufacturer, Exporter to the US, Manufacturer, Remanufacturer, Repackager or relabeler, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Hue Light Co., Ltd | Gwangmyeong-si Gyeonggi, South Korea | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Johnson Health Tech (shanghai) Co., Ltd. | Jiading Shanghai, China | Exporter to the US, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Lode B.V. | Groningen, Netherlands | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Medical Graphics Corp. | Saint Paul, MN, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Motek Medical B.V. | Houten Noord-Brabant, Netherlands | Complaint file establishment, Manufacturer, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Mobility Research | Phoenix, AZ, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| P&S Robotics Co.,ltd | Seoul, South Korea | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Reha-Stim Medtec GMBH | Berlin, Germany | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Sport Medical Technology Inc | Shirley, NY, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Tianjin Goldenall Medical Device Co.,ltd | Tianjin city, China | Exporter to the US, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Woodway Usa, Inc. | Vernon, WI, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Zhejiang Todo Hardware Manufacture Co.,ltd | Jinhua Zhejiang, China | Contract manufacturer, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated September 6, 1995. 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.