Data / Medical devices / Chair, Geriatric
Chair, Geriatric (FRJ): 22 FDA-registered makers in 6 countries
22 establishments in 6 countries are registered with the FDA to make Chair, Geriatric (product code FRJ, Class 1, 21 CFR 880.6140). 0 of them have a 510(k) clearance or PMA approval on file and 0 have a recall event. The FDA has issued 0 510(k) clearances under this code, and lists 1 recall event (0 Class I). FDA data exported November 2, 2026.
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- Product code
- FRJ
- Device class
- 1
- Regulation
- 880.6140
- Medical specialty
- General Hospital
Makers by country
| Country | Makers |
|---|---|
| China | 11 |
| United States | 5 |
| Canada | 2 |
| Taiwan | 2 |
| Mexico | 1 |
| India | 1 |
Makers of Chair, Geriatric
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 |
|---|---|---|---|---|---|---|---|---|
| A & I Industries Ltd | FOSHAN CITY Guangdong, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Broda LP | Kitchener Ontario, Canada | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Champion MFG, INC. | Ocala, FL, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Danyang Huayi Medical Supply & Equipment Co, Ltd | DANYANG Jiangsu, China | Contract manufacturer, Exporter to the US, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Healthline Medical Products | Winter Garden, FL, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Innovative Products Unlimited, Inc. | Niles, MI, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Jiangsu Pinkang Medical Technology Co Ltd | Danyang Jiangsu, China | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Jiangyin Unixcare Medical Devices Co.,ltd | Jiangyin Jiangsu, China | Exporter to the US, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Jiaxing Kalanchoe Medical Technology Co., Ltd | Jiaxing Zhejiang, China | Contract manufacturer, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Jan Mao Industries Co., Ltd. | Guangxi Zhuang Autonomous Region, China | Exporter to the US, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Jiangsu Intco Medical Products Co., Ltd. | Zhenjiang New District Jiangsu, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Jiangyin Huashi Medical Equipment Co.,Ltd | Jiangyin City Jiangsu, China | 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 | |
| New Allied Corporation | Taichung City, Taiwan | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Sigma-Care Development Co., Ltd. | Dalin Township, Chiayi County Chiayi(County), Taiwan | Exporter to the US, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Surface Medical, Inc. | Calgary Alberta, Canada | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Tynor Orthotics (P) Ltd. | Mohali Punjab, India | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Yongkang Beiqin Industry & Trade Co.,ltd | Yongkang Zhejiang, China | Exporter to the US, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Zhejiang Kelongwei Medical Equipment Co., Ltd. | Shaoxing Zhejiang, China | Contract manufacturer, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Zhongshan A&j Medical Equipment Co., Ltd. (JBS) | Zhongshan City Guangdong, China | Manufacturer | 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.