Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3013654075

FEI Number

3013654075

Entity Name

SHEN ZHEN GREAT FORCE PLASTIC PRODUCTS CO.LTD

City/State/Country

Shenzhen Guangdong, CN

Establishment Address

No. 4 Baoxilu, Kengzi, Pingshan, Shenzhen Guangdong 518122, CN

Establishment Type(s)

Repack or Relabel Medical Device,Manufacture Medical Device,Manufacture Medical Device for Another Party (Contract Manufacturer),Complaint File Establishment per 21 CFR 820.198

Owner / Operator

Shen Zhen Great Force Plastic Products Co.Ltd (Owner Number: 10062161)

Owner / Operator Contact Address

No. 4 Baoxilu, Kengzi, Pingshan, Shenzhen, CN-GD 518122, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
FHA	Clamp, Penile	Gastroenterology, Urology	Class 1	876.5160	2020-07-23

Official Correspondent

Yihe Chen

US Agent Details

Emily Matorin Business: FDAbasics Email: usagent@fdabasics.com Phone: (716) 7750533

Related Public Records

Same Entity

Shen Zhen Great Force Plastic Products 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 3013654075. Last updated year: 2026. Please use registration number 3013654075 when referencing this establishment in official correspondence.