Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3012292909

FEI Number

3012292909

Entity Name

Yuhuan City Shengbo Mould Manufacturing Co.,Ltd.

City/State/Country

Yuhuan Zhejiang, CN

Establishment Address

Western of Chinese Sterile Medical Equipment Base,Qinggang Town, Yuhuan Zhejiang 317606, CN

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

Yuhuan City Shengbo Mould Manufacturing Co.,Ltd. (Owner Number: 10051317)

Owner / Operator Contact Address

Western of Chinese Sterile Medical Equipment Base,Qinggang Town, Yuhuan, CN-ZJ 317606, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Tweezer/Forceps Speculums

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
KCX	Epilator, High Frequency, Tweezer-Type	General, Plastic Surgery	Class 1	878.5360	2024-04-22
HIB	Speculum, Vaginal, Nonmetal	Obstetrics/Gynecology	Class 2	884.4530	2016-03-02

Official Correspondent

No official correspondent registered.

US Agent Details

Mukesh Kumar Business: Brij Strategic Consultations, LLC Email: mkumar@FDAMap.com Phone: (240) 7504893

Related Public Records

Same Entity

Yuhuan City Shengbo Mould Manufacturing 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 3012292909. Last updated year: 2026. Please use registration number 3012292909 when referencing this establishment in official correspondence.