Data / Medical devices / China / Wujiang City Cloud & Dragon Medical Device Co., Ltd
Wujiang City Cloud & Dragon Medical Device Co., Ltd: FDA-registered device maker in Suzhou Jiangsu, China, 2 510(k) clearances
Wujiang City Cloud & Dragon Medical Device Co., Ltd is registered with the FDA (registration 8044116) in Suzhou Jiangsu, China. It lists 4 device types. The FDA files 2 510(k) clearances under its listings, the newest dated December 2, 2013. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 8044116
- FEI number
- 3004374580
- Address
- West of Building FS-02, 807 West Ganquan Road, Jiangling Street, Wujiang District, Suzhou Jiangsu, China, 215200
- Owner or operator
- WUJIANG CITY CLOUD & DRAGON MEDICAL DEVICE CO. LTD (9005662)
- Roles
- Contract manufacturer, Manufacturer
- First device listed
- April 25, 2008
- Registered through
- 2026
- Brand names listed
- Acuregen; Carbo; NANO TECH: OPTIMED; Thrive: ProMaxx, Dao Needle; Longevity, Balance, Tempo, Cloud & Dragon, Cloud & Dragon Acupuncture Needles, Acupotomy Acupuncture Needles, Acutomo Needles, Facial Needles,, Cloud & Dragon Press Needles Interadermal Embedding Needles, Dermal Needles, Seven Star Skin Needles; Ear Needles,, Cloud & Dragon, Expert, LEKON, Detox Needles, Hand Sujok Needles, Dry Needling Needles, Ear Seeds, Auricular Point Sticker, Vaccaira Ear Seeds, Magnetic Plaster Patch, Kinesiology Sports Tape, Tape Cutter, Facial Cupping Cups, Cupping Suction Pump and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Device, Pressure Applying | KNM | 1 | Manufacturer | accessdata.fda.gov |
| Needle, Acupuncture, Single Use | MQX | 2 | Contract manufacturer, Manufacturer | accessdata.fda.gov |
| Pack, Heat, Moist | IMA | 1 | Manufacturer | accessdata.fda.gov |
| Tape And Bandage, Adhesive | KGX | 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 |
|---|---|---|---|---|---|---|
| December 2, 2013 | K132896 | CJ-TYPE: METAL HANDLE WITH GUIDE TUBE, PJ-TYPE: PLASTIC HANDLE WITH GUIDE TUBE, CB-TYPE: METAL HANDLE WITHOUT GUIDE TUBE | MQX | Substantially Equivalent | Asia-Med GmbH and CO KG | accessdata.fda.gov |
| April 24, 1997 | K970574 | ACUPUNCTURE NEEDLES | MQX | Substantially Equivalent | C.A.I. Industries Corp. | accessdata.fda.gov |
Compare with other makers
- All makers of Needle, Acupuncture, Single Use
- All makers of Pack, Heat, Moist
- All makers of Tape And Bandage, Adhesive
- All makers of Device, Pressure Applying
Updated December 2, 2013. 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.