Shenzhenshi Sincoheren S&T Development Co., Ltd.

Brand owner, China. 4 products catalogued, 2 clearances.

Registry build 21.09.26

Shenzhenshi Sincoheren S&T Development Co., Ltd. holds an FDA establishment registration in China. Its registration names no device type; it is in this index because it catalogues devices under its own name. 4 of its products are catalogued under its own name.

4products catalogued under its own name
2510(k) clearances

Registration

FDA registration record for Shenzhenshi Sincoheren S&T Development Co., Ltd.
Status Not current
DUNS 706040997

Location

Address of Shenzhenshi Sincoheren S&T Development Co., Ltd.
Country China

Own-Brand Listings

Devices catalogued by Shenzhenshi Sincoheren S&T Development Co., Ltd.
Product Code Catalogue numbers
LED Spectrum therapy instrument GEX 5
Microneedle electrodes GEI 2
RF electrodes GEI 1
Radio Frequency System GEI 1

Clearances

510(k) clearances naming Shenzhenshi Sincoheren S&T Development Co., Ltd. or its listings
Clearance Decision date Product code Route Held by
K231749 2023-10-19 GEI Traditional This company
K231894 2023-09-20 GEX Traditional This company

Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.

The manufacturer named here can complete this record.

Where China Actually Supplies

Every device page names the company that lists it and the factories registered to make the same thing. These are the sections with the most of them.

5,100manufacturers registered in China
2,581device types they are registered for
340,248device records, each naming its maker
31provinces with a registered manufacturer