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Sign in to claim this brandShenzhen Wikkon Precision Technologies Co., Ltd.
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Last updated May 31, 2026
What Shenzhen Wikkon Precision Technologies Co., Ltd. makes
Shenzhen Wikkon Precision Technologies Co., Ltd. makes extracorporeal electromechanical lithotripsy systems, specifically extracorporeal shock wave lithotripters, including the U200 model. These devices are used to break down kidney stones using focused shock waves generated outside the body.
The company's devices are classified as Class II medical devices and are listed in the FDA 510(k) database and the FDA Unique Device Identification (UDI) system. Shenzhen Wikkon Precision Technologies Co., Ltd. is based in the United States.
Written from this company's registered devices by an AI model, and not verified by a human reviewer.
Frequently asked questions
What type of medical devices does Shenzhen Wikkon Precision Technologies manufacture?
Shenzhen Wikkon Precision Technologies produces extracorporeal electromechanical lithotripsy systems, specifically extracorporeal shock wave lithotripters such as the standard model and the U200. This conclusion comes directly from the device categories and example devices listed in the provided data.
Where is Shenzhen Wikkon Precision Technologies based?
The company is based in the United States, as indicated by the COUNTRY field in the supplied information. No other location is mentioned, so the U.S. is the only confirmed base of operations.
In which FDA registries are the company's lithotripters listed?
The lithotripters are listed in the FDA 510(k) database and the FDA Unique Device Identification (UDI) system. This is explicitly stated under the LISTED IN section, confirming that both registries contain entries for the company's devices.
How are Shenzhen Wikkon Precision Technologies' lithotripters classified under FDA regulations?
All of the company's extracorporeal shock wave lithotripters are classified as Class II medical devices. The DEVICE CLASSES entry specifies Class II, indicating the regulatory risk level and the type of controls applicable to these devices.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
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- Website
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- Phone
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- PRRC Contact
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- EUDAMED SRN
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- FDA FEI Number
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- DUNS Number
- 543036260
Catalogue (2)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Extracorporeal Shock Wave Lithotripter | U200 | FDA UDI | Class II | Active |
| Extracorporeal Shock Wave Lithotripter (U200) | K242922 | FDA 510(k) | Class II | Active |
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FDA Establishments (1)
Establishments registered with the FDA under this company group, matched by name.
- Shenzhen Wikkon Precision Technologies Co., Ltd. Shenzhen Guangdong · CN FEI 3040388525