Data / Medical devices / China / WickiMed (Huizhou) Medical Equipment Manufacturing Co., Ltd.
WickiMed (Huizhou) Medical Equipment Manufacturing Co., Ltd.: FDA-registered device maker in HuiZhou Guangdong, China, 1 510(k) clearance
WickiMed (Huizhou) Medical Equipment Manufacturing Co., Ltd. is registered with the FDA (registration 3020142587) in HuiZhou Guangdong, China. It lists 2 device types. The FDA files 1 510(k) clearance under its listings, the newest dated April 28, 2010. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3020142587
- Address
- 5th Floor, Building D, No.3 Nandi Road, Yingguang Village, Lilin Town, Zhongkai High-Tech Zone, HuiZhou Guangdong, China, 516035
- Owner or operator
- Wickimed Supply Co., Ltd. (10029747)
- Roles
- Contract manufacturer, Contract sterilizer, Manufacturer
- First device listed
- September 15, 2011
- Registered through
- 2026
- Brand names listed
- 3cm TUNGSTEN MICRONEEDLE(Model:138505,138505-10), 45 degree TUNGSTEN MICRONEEDLE(Model:138504,138504-10), 4cm TUNGSTEN MICRONEEDLE(Model:138506,138506-10), Electrosurgical Pencil with electrode,model:WP200,WP200-B100S,WP200-C100S,WP200-L31S,WP200-N100S,WP200-B90S
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Apparatus, Exhaust, Surgical | FYD | 2 | Contract manufacturer, Contract sterilizer | accessdata.fda.gov |
| Electrosurgical, Cutting & Coagulation & Accessories | GEI | 2 | Contract manufacturer, Contract sterilizer, 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 |
|---|---|---|---|---|---|---|
| April 28, 2010 | K100258 | ELECTROSURGICAL PENCIL WITH ELECTRODE, WP200 | GEI | Substantially Equivalent | Wickimed Supply Limited | accessdata.fda.gov |
Compare with other makers
- All makers of Electrosurgical, Cutting & Coagulation & Accessories
- All makers of Apparatus, Exhaust, Surgical
Updated April 28, 2010. 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.