Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3043639843

FEI Number

3043639843

Entity Name

GUANGZHOU HEHONG BIOTECH CO., LTD.

City/State/Country

Guangzhou Guangdong, CN

Establishment Address

A zone, 2/F, Building A, Huazi Industrial Park,, Shilou Town, Panyu District, Guangzhou Guangdong 511447, CN

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Guangzhou Hehong Biotech Co., Ltd. (Owner Number: 10093562)

Owner / Operator Contact Address

A zone, 2/F, Building A, Huazi Industrial Park,, Shilou Town, Panyu District, Guangzhou, CN-GD 511447, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K253354

PMA Number

N/A

All Registered Proprietary Names

Minvitro Vitrification Straw Minvitro

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
MQK	Labware, Assisted Reproduction	Obstetrics/Gynecology	Class 2	884.6160	2026-01-12
MQF	Catheter, Assisted Reproduction	Obstetrics/Gynecology	Class 2	884.6110	2026-02-26

Official Correspondent

No official correspondent registered.

US Agent Details

Jessie Yao Business: MEDRIGHT TECH INC Email: info@medright-tech.com Phone: (718) 2169957

Related Public Records

Same Entity

Guangzhou Hehong Biotech Co., Ltd.

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

View Entity Profile →

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K112396	Kitazato Medical Co., Ltd.	IUI CATHETERS	2012-11-02

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3043639843. Last updated year: 2026. Please use registration number 3043639843 when referencing this establishment in official correspondence.