Wujiang Jiachen Acupuncture Devices Co., Ltd.

Registered establishment in Suzhou City, Jiangsu Province, China. 1 device type.

Registry build 21.09.26

Wujiang Jiachen Acupuncture Devices Co., Ltd. is a manufacturer holding a current FDA establishment registration. The registration covers Needle, Acupuncture, Single Use. Its earliest product listing with the FDA dates from 2007.

Registration

FDA registration record for Wujiang Jiachen Acupuncture Devices Co., Ltd.
Registered name WUJIANG JIACHEN ACUPUNCTURE DEVICES CO., LTD.
Status Registered
Registration expires 2026
Registration number 3003903033
FEI number 3003903033
Establishment type Manufacturer

Chinese Registration

Chinese company register details for Wujiang Jiachen Acupuncture Devices Co., Ltd.
Chinese legal name 吴江市佳辰针灸器械有限公司
Source Qichacha company register

Location

Address of Wujiang Jiachen Acupuncture Devices Co., Ltd.
City Suzhou City, Jiangsu Province
Address NO.37 LIMIN SOUTH RD.,
Postal code 215212
Country China

What It Makes

Device types Wujiang Jiachen Acupuncture Devices Co., Ltd. is registered to make
Device type Class Listed under the names Listed since Chinese makers
Needle, Acupuncture, Single Use Class 2 Motion, CopperStar, EAR Press Needle, Facial Needles, Bleeding Needle, Pine, Silverstar, Unisharp and 4 more 2007 33

Clearances

No clearance names Wujiang Jiachen Acupuncture Devices Co., Ltd. as applicant. One is held by another company and named on this establishment’s own product listings: the device is cleared under that company’s 510(k) and listed under this registration.

510(k) clearances naming Wujiang Jiachen Acupuncture Devices Co., Ltd. or its listings
Clearance Decision date Product code Route Held by
K023054 2002-11-13 MQX Traditional Mandala Health Care, LLC

From the Company

Published by the company on its own website, not by the FDA.

Information published by Wujiang Jiachen Acupuncture Devices Co., Ltd.
Founded 1999
Main products Sterile acupuncture needles, Press needles, Ear seeds, Seven-star needles, Acupuncture models
Certifications ISO13485, CE, MDSAP, FDA, TGA
Export markets Over 50 countries worldwide
OEM and ODM Offered

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