Data / Medical devices / China / Shenzhen Shine Industrial Co., Ltd.
Shenzhen Shine Industrial Co., Ltd.: FDA-registered device maker in Shenzhen Guangdong, China, 1 510(k) clearance
Shenzhen Shine Industrial Co., Ltd. is registered with the FDA (registration 3006026335) in Shenzhen Guangdong, China. It lists 2 device types. The FDA files 1 510(k) clearance under its listings, the newest dated April 9, 2012. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3006026335
- Address
- Bldg 10, 1st Industrial Zone,Changzhen Community Guangming District, Shenzhen Guangdong, China, 518132
- Owner or operator
- Shenzhen Shine Industrial Co., Ltd. (9091659)
- Roles
- Manufacturer
- First device listed
- April 22, 2012
- Registered through
- 2026
- Brand names listed
- BA15081CB (WW715ZFPDQ), BA15091 (WW702F), BA16121 (WW709F), Body Analyser BA15081 (WW702XF), Body Analyser BA15081 (WW718XF), Body Analyser BA15091 (WW712XF), Body Analyser BA16121 (WW709XF), Body analyzer BS0106(WW52N) and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Analyzer, Body Composition | MNW | 2 | Manufacturer | accessdata.fda.gov |
| Analyzer, Body Composition, Exempt | PUH | 2 | 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 |
|---|---|---|---|---|---|---|
| April 9, 2012 | K112149 | WEIGHT AND BODY FAT SCALE SHINE BS0105 | MNW | Substantially Equivalent | Shine Overseas Marketing Limited | accessdata.fda.gov |
Compare with other makers
Updated April 9, 2012. 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.