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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

CountryMakers
United States7
China5
India2
Germany2
South Korea2
Netherlands2
Taiwan1
Israel1

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.

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Advanced Mechanical Technology IncWatertown, MA, United StatesManufacturer0000api.fda.gov
Apothecaries Sundries MFG Pvt LtdGURUGRAM Haryana, IndiaManufacturer, Repackager or relabeler0000api.fda.gov
Body Charger Fitness Int'l Corp(gee Hoo Fitec Corp)Yuanlin City Changhua, TaiwanManufacturer0000api.fda.gov
Edan Instruments, Inc.Shenzhen Guangdong, ChinaManufacturer0000api.fda.gov
Ekso BionicsSan Rafael, CA, United StatesComplaint file establishment, Manufacturer0000api.fda.gov
Full Vision, Inc.Newton, KS, United StatesManufacturer0020api.fda.gov
Fourier Intelligence Inc.Shanghai, ChinaManufacturer0000api.fda.gov
Goldengait Ltd.Bnei Brak Central, IsraelManufacturer0000api.fda.gov
Greens Surgicals Private LimitedVadodara Gujarat, IndiaManufacturer0000api.fda.gov
H/P/Cosmos Sports & Medical GMBHNUSSDORF BEI TRAUNSTEIN Bavaria, GermanyContract manufacturer, Exporter to the US, Manufacturer, Remanufacturer, Repackager or relabeler, Specification developer0000api.fda.gov
Hue Light Co., LtdGwangmyeong-si Gyeonggi, South KoreaManufacturer0000api.fda.gov
Johnson Health Tech (shanghai) Co., Ltd.Jiading Shanghai, ChinaExporter to the US, Manufacturer0000api.fda.gov
Lode B.V.Groningen, NetherlandsManufacturer0000api.fda.gov
Medical Graphics Corp.Saint Paul, MN, United StatesSpecification developer0000api.fda.gov
Motek Medical B.V.Houten Noord-Brabant, NetherlandsComplaint file establishment, Manufacturer, Specification developer0000api.fda.gov
Mobility ResearchPhoenix, AZ, United StatesManufacturer0000api.fda.gov
P&S Robotics Co.,ltdSeoul, South KoreaManufacturer0000api.fda.gov
Reha-Stim Medtec GMBHBerlin, GermanyManufacturer0000api.fda.gov
Sport Medical Technology IncShirley, NY, United StatesManufacturer0000api.fda.gov
Tianjin Goldenall Medical Device Co.,ltdTianjin city, ChinaExporter to the US, Manufacturer0000api.fda.gov
Woodway Usa, Inc.Vernon, WI, United StatesManufacturer0000api.fda.gov
Zhejiang Todo Hardware Manufacture Co.,ltdJinhua Zhejiang, ChinaContract manufacturer, Manufacturer0000api.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.