Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3040388525

FEI Number

3040388525

Entity Name

SHENZHEN WIKKON PRECISION TECHNOLOGIES CO., LTD.

City/State/Country

Shenzhen Guangdong, CN

Establishment 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 518038, CN

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Shenzhen Wikkon Precision Technologies Co., Ltd. (Owner Number: 10093865)

Owner / Operator Contact 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, CN-GD 518038, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K242922

PMA Number

N/A

All Registered Proprietary Names

Extracorporeal Shock Wave Lithotripter (U200)

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
LNS	Lithotriptor, Extracorporeal Shock-Wave, Urological	Gastroenterology, Urology	Class 2	876.5990	2025-07-24

Official Correspondent

Yanbo Wang

US Agent Details

John Hoffer Business: DORNIER MEDTECH AMERICA, INC Email: Jhoffer@Dornier.com Phone: (770) 5146163

Related Public Records

Same Entity

Shenzhen Wikkon Precision Technologies Co., Ltd.

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3040388525. Last updated year: 2026. Please use registration number 3040388525 when referencing this establishment in official correspondence.