Data / Medical devices / Bars, Parallel, Exercise
Bars, Parallel, Exercise (IOE): 14 FDA-registered makers in 6 countries
14 establishments in 6 countries are registered with the FDA to make Bars, Parallel, Exercise (product code IOE, Class 1, 21 CFR 890.5370). 0 of them have a 510(k) clearance or PMA approval on file and 0 have a recall event. The FDA has issued 2 510(k) clearances under this code, the latest on March 9, 1983, and lists 0 recall events (0 Class I). FDA data exported November 2, 2026.
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- Product code
- IOE
- Device class
- 1
- Regulation
- 890.5370
- Medical specialty
- Physical Medicine
Makers by country
| Country | Makers |
|---|---|
| United States | 7 |
| China | 3 |
| Germany | 1 |
| Hong Kong | 1 |
| Mexico | 1 |
| Pakistan | 1 |
Makers of Bars, Parallel, Exercise
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 |
|---|---|---|---|---|---|---|---|---|
| Armedica MFG. | Greenwood, AR, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Clinton Industries, Inc | York, PA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Djo, LLC | Carlsbad, CA, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Dong Guan Yunzhishang Health Technology Co.,ltd. | Dongguan City Guangdong, China | 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 | |
| Hangzhou Zhongzhi Industry Co.,ltd | Hangzhou Zhejiang, China | Exporter to the US, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Hausmann Enterprises, LLC | Northvale, NJ, United States | Manufacturer, Repackager or relabeler | 0 | 0 | 0 | 0 | api.fda.gov | |
| IPE Plastic & Hardware Industy, LTD | Dongguan Guangdong, China | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Jasan International Limited | Hong Kong, Hong Kong | Exporter to the US, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| MCR Internacional SA De CV | REYNOSA Tamaulipas, Mexico | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| MJM International Corporation | Edinburg, TX, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Mor-Medical International | Pharr, TX, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Pivotal Health Solutions | Watertown, SD, United States | Complaint file establishment, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Stone Instruments Co. | SIALKOT Punjab, Pakistan | Contract manufacturer, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated March 9, 1983. 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.