Data / Medical devices / China / Shenzhen Healthcare Electronic Technology Co., Ltd.
Shenzhen Healthcare Electronic Technology Co., Ltd.: FDA-registered device maker in Shenzhen Guangdong, China, 3 510(k) clearances
Shenzhen Healthcare Electronic Technology Co., Ltd. is registered with the FDA (registration 3006624940) in Shenzhen Guangdong, China. It lists 4 device types. The FDA files 3 510(k) clearances under its listings, the newest dated June 28, 2012. Registered through 2026. FDA data exported November 3, 2026.
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- FDA registration number
- 3006624940
- Address
- Block 48, Changxing Industrial Zone, Changzhen,Gongming Town Guangming District, Shenzhen Guangdong, China, 518132
- Owner or operator
- SHENZHEN HEALTHCARE ELECTRONIC TECHNOLOGY CO., LTD. (10037620)
- Roles
- Manufacturer
- First device listed
- August 1, 2011
- Registered through
- 2026
- Brand names listed
- Bluetooth Body Analysis Scale, WW930XF, Bluetooth® Digital Body Composition Scale, Model number: 32910034,13635, Body Analysis Scale, Multiple Models, Body Fat Scale, 5298578, Body analysis scale, Multiple Models, Digital Body Composition Scale, Model number: 32910032,13633, Face and Body Massager, TY BH BIA GLS 2 TONE BLK SLVR 3 TRY WAL, Model 5329325 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 |
| Massager, Therapeutic, Electric | ISA | 1 | Manufacturer | accessdata.fda.gov |
| Scale, Stand-On, Patient | FRI | 1 | 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 |
|---|---|---|---|---|---|---|
| June 28, 2012 | K121527 | WI-FI BODY SCALE | MNW | Substantially Equivalent | Shenzhen Healthcare Electronic Technology Co., Ltd. | accessdata.fda.gov |
| November 1, 2011 | K112951 | BODY ANALYSIS SCALE | MNW | Substantially Equivalent | Shenzhen Healthcare Electronic Technology Co., Ltd. | accessdata.fda.gov |
| July 15, 2011 | K110928 | BODY ANALYSIS SCALE, MODEL BG 17 | MNW | Substantially Equivalent | Shenzhen Healthcare Electronic Technology Co., Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Analyzer, Body Composition, Exempt
- All makers of Analyzer, Body Composition
- All makers of Scale, Stand-On, Patient
- All makers of Massager, Therapeutic, Electric
Updated June 28, 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.