Data / Medical devices / China / Shenzhen Wikkon Precision Technologies Co., Ltd.
Shenzhen Wikkon Precision Technologies Co., Ltd.: FDA-registered device maker in Shenzhen Guangdong, China, 1 510(k) clearance
Shenzhen Wikkon Precision Technologies Co., Ltd. is registered with the FDA (registration 3040388525) in Shenzhen Guangdong, China. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated June 18, 2025. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3040388525
- Address
- Room 1503, 15th Floor, Building A, Chuanglingtong Science and Technology Building, No.1 Shihua Road Futian Bonded Area, Shenzhen City, Guangdong Province, China, Shenzhen Guangdong, China, 518038
- Owner or operator
- Shenzhen Wikkon Precision Technologies Co., Ltd. (10093865)
- Roles
- Manufacturer
- First device listed
- July 24, 2025
- Registered through
- 2026
- Brand names listed
- Extracorporeal Shock Wave Lithotripter (U200)
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Lithotriptor, Extracorporeal Shock-Wave, Urological | LNS | 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 |
|---|---|---|---|---|---|---|
| June 18, 2025 | K242922 | Extracorporeal Shock Wave Lithotripter (U200) | LNS | Substantially Equivalent | Shenzhen Wikkon Precision Technologies Co., Ltd. | accessdata.fda.gov |
Compare with other makers
Updated June 18, 2025. 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.