FOSHAN KING WONDER HI-TECH CO.,LTD.

FDA Device Registration & Listing · Foshan Guangdong, CN · Registration 3022121576

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3022121576
FEI Number
3022121576
Entity Name
FOSHAN KING WONDER HI-TECH CO.,LTD.
City/State/Country
Foshan Guangdong, CN
Establishment Address
Block 3, No.6 Yongye Road, Yundonghai Street, Sanshui District, Foshan Guangdong 528100, CN
Establishment Type(s)
Manufacture Medical Device,Export Device to the United States But Perform No Other Operation on Device,Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
Foshan King Wonder Hi-Tech Co.,LTD. (Owner Number: 10084460)
Owner / Operator Contact Address
Block 3, No.6 Yongye Road, Yundonghai Street, Sanshui District, Foshan, CN-GD 528100, CN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Urosecure Foly catheter securement device Vasette external catheter device Qivi acute male external urine management

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
EYJ Holder, Ureteral Catheter Gastroenterology, Urology Class 1 876.5130 2022-02-24
NZU Collector, Urine, Powered, Non Indwelling Catheter Gastroenterology, Urology Class 1 876.5250 2023-06-21

Official Correspondent

No official correspondent registered.

US Agent Details

David Lennarz Business: Registrar Corp Email: david.lennarz@registrarcorp.com Phone: (757) 2240177

Related Public Records

Same Entity

Foshan King Wonder Hi-Tech 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 3022121576. Last updated year: 2026. Please use registration number 3022121576 when referencing this establishment in official correspondence.
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