Data / Medical devices / China / Foshan Kaiyang Medical Equipment Co., Ltd.
Foshan Kaiyang Medical Equipment Co., Ltd.: FDA-registered device maker in Foshan City Guangdong, China, 3 510(k) clearances
Foshan Kaiyang Medical Equipment Co., Ltd. is registered with the FDA (registration 3007120364) in Foshan City Guangdong, China. It lists 9 device types. The FDA files 3 510(k) clearances under its listings, the newest dated October 4, 2010. Registered through 2027. FDA data exported November 2, 2026.
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- FDA registration number
- 3007120364
- Address
- 3 of No. 21, The 3rd Hongling Road, Shishan Town Nanhai District, Foshan City Guangdong, China, 528231
- Owner or operator
- Foshan Kaiyang Medical Equipment Co., Ltd. (10026314)
- Roles
- Exporter to the US, Manufacturer
- First device listed
- July 2, 2008
- Registered through
- 2027
- Brand names listed
- Cane, Holder, Crutch and Cane, Wheelchair, Hygiene Products, Manual Bed, Mechanical Chair, Mechanical Walker, Mechanical Wheelchair, Powered Hospital Bed and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Adaptor, Hygiene | ILS | 1 | Exporter to the US, Manufacturer | accessdata.fda.gov |
| Attachment, Commode, Wheelchair | INB | 1 | Exporter to the US, Manufacturer | accessdata.fda.gov |
| Bed, Ac-Powered Adjustable Hospital | FNL | 2 | Exporter to the US, Manufacturer | accessdata.fda.gov |
| Bed, Manual | FNJ | 1 | Exporter to the US, Manufacturer | accessdata.fda.gov |
| Cane | IPS | 1 | Exporter to the US, Manufacturer | accessdata.fda.gov |
| Chair, Adjustable, Mechanical | INN | 1 | Exporter to the US, Manufacturer | accessdata.fda.gov |
| Holder, Crutch And Cane, Wheelchair | IMZ | 1 | Exporter to the US, Manufacturer | accessdata.fda.gov |
| Walker, Mechanical | ITJ | 1 | Exporter to the US, Manufacturer | accessdata.fda.gov |
| Wheelchair, Mechanical | IOR | 1 | Exporter to the US, Manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| October 4, 2010 | K101999 | KAIYANG STEEL WHEELCHAIR | IOR | Substantially Equivalent | Guangdong Kaiyang Medical Technology Co., Ltd. | accessdata.fda.gov |
| October 4, 2010 | K101998 | KAIYANG ALUMINUM WHEELCHAIR | IOR | Substantially Equivalent | Guangdong Kaiyang Medical Technology Co., Ltd. | accessdata.fda.gov |
| January 12, 2001 | K003783 | MEDICAL DEPOT-WHEELCHAIRS, MODEL SENTRA,ASTAIRE AND VIPER | IOR | Substantially Equivalent | Medical Depot, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Wheelchair, Mechanical
- All makers of Adaptor, Hygiene
- All makers of Attachment, Commode, Wheelchair
- All makers of Holder, Crutch And Cane, Wheelchair
- All makers of Cane
- All makers of Chair, Adjustable, Mechanical
Updated October 4, 2010. 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.