Data / Medical devices / China / Shaoxing Yingtuo Healthcare Co.,ltd.
Shaoxing Yingtuo Healthcare Co.,ltd.: FDA-registered device maker in Shaoxing Zhejiang, China, 1 510(k) clearance
Shaoxing Yingtuo Healthcare Co.,ltd. is registered with the FDA (registration 3015429360) in Shaoxing Zhejiang, China. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated August 31, 2021. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3015429360
- Address
- NO.11 Tengda Road,Cao E Street,Shangyu Area, Shaoxing Zhejiang, China, 312000
- Owner or operator
- Shaoxing Yingtuo Healthcare Co.,Ltd. (10060327)
- Roles
- Manufacturer
- First device listed
- September 13, 2021
- Registered through
- 2026
- Brand names listed
- adhesive electrode
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Electrode, Cutaneous | GXY | 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 |
|---|---|---|---|---|---|---|
| August 31, 2021 | K210448 | Adhesive Electrode | GXY | Substantially Equivalent | Shaoxing Yingtuo Healthcare Co., Ltd. | accessdata.fda.gov |
Compare with other makers
Updated August 31, 2021. 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.