Data / Medical devices / China / Wujiang Jiachen Acupuncture Devices Co., Ltd.
Wujiang Jiachen Acupuncture Devices Co., Ltd.: FDA-registered device maker in Suzhou City, Jiangsu Province, China, 1 510(k) clearance
Wujiang Jiachen Acupuncture Devices Co., Ltd. is registered with the FDA (registration 3003903033) in Suzhou City, Jiangsu Province, China. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated November 13, 2002. Registered through 2026. FDA data exported November 3, 2026.
SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.
- FDA registration number
- 3003903033
- Address
- No.37 Limin South RD., Lili Town, Wujiang District, Suzhou City, Jiangsu Province, China, 215212
- Owner or operator
- WUJIANG JIACHEN ACUPUNCTURE DEVICES CO., LTD. (9052962)
- Roles
- Manufacturer
- First device listed
- May 25, 2007
- Registered through
- 2026
- Brand names listed
- Acupoint, CopperStar, EAR PRESS NEEDLE, FACIAL NEEDLES, BLEEDING NEEDLE, HyChi, Motion, PINE, SILVERSTAR, Starlite and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Needle, Acupuncture, Single Use | MQX | 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 |
|---|---|---|---|---|---|---|
| November 13, 2002 | K023054 | JIA CHEN ACUPUNCTURE NEEDLE, FOR SINGLE USE | MQX | Substantially Equivalent | Mandala Health Care, LLC | accessdata.fda.gov |
Compare with other makers
Updated November 13, 2002. 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.