Data / Medical devices / China / Foshan Dongfang Medical Equipment Manufactory(ltd)
Foshan Dongfang Medical Equipment Manufactory(ltd): FDA-registered device maker in FOSHAN Guangdong, China, 1 510(k) clearance
Foshan Dongfang Medical Equipment Manufactory(ltd) is registered with the FDA (registration 3004194020) in FOSHAN Guangdong, China. It lists 14 device types. The FDA files 1 510(k) clearance under its listings, the newest dated July 20, 2004. Registered through 2027. FDA data exported November 3, 2026.
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- FDA registration number
- 3004194020
- Address
- No.5 Xingfu RD. Nanhai Shisan Industrial Park, FOSHAN Guangdong, China, 528225
- Owner or operator
- FOSHAN DONGFANG MEDICAL EQUIPMENT MANUFACTORY(LTD) (9059383)
- Roles
- Contract manufacturer, Manufacturer
- First device listed
- October 29, 2003
- Registered through
- 2027
- Brand names listed
- ATTACHMENT, COMMODE, WHEELCHAIR, BATH BENCH ; COMMODE, CANE, CRUTCH, ELECTRIC BEDS, IV STAND, MECHANICAL TABLE, MECHANICAL WALKER and more
Devices it lists
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 |
|---|---|---|---|---|---|---|
| July 20, 2004 | K041814 | FS SERIES WHEELCHAIR | IOR | Substantially Equivalent | Foshan Dongfang Medical Equipment Manufactory(Ltd) | accessdata.fda.gov |
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Updated July 20, 2004. 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.