Data / Medical devices / Hong Kong / Wickimed Supply Company Limited.
Wickimed Supply Company Limited.: FDA-registered device maker in Hong Kong, Hong Kong, 2 510(k) clearances
Wickimed Supply Company Limited. is registered with the FDA (registration 3007710878) in Hong Kong, Hong Kong. It lists 1 device type. The FDA files 2 510(k) clearances 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
- 3007710878
- Address
- Room317, 3/F, Genplas Industrial Building, 56 Hoi Yuen Road, Kwun Tong,Kowloon, Hong Kong, Hong Kong, 999077
- Owner or operator
- Wickimed Supply Co., Ltd. (10029747)
- Roles
- Exporter to the US
- First device listed
- June 23, 2009
- 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 |
|---|---|---|---|---|
| Electrosurgical, Cutting & Coagulation & Accessories | GEI | 2 | Exporter to the US | 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 |
| February 22, 1994 | K932654 | ELECTROSURGIAL INSTRUMENTS | GEI | Substantially Equivalent | Medline Industries, Inc. | accessdata.fda.gov |
Compare with other makers
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.