Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3014326210

FEI Number

3014326210

Entity Name

Guangzhou Zhongshu E-Commerce Co., Ltd.

City/State/Country

Guangzhou Guangdong, CN

Establishment Address

Room 111, Building 7, No. 96, Rd. Lixin 12, Xintang Town, Zengcheng District, Guangzhou Guangdong 511300, CN

Establishment Type(s)

Export Device to the United States But Perform No Other Operation on Device

Owner / Operator

Guangzhou Zhongshu E-Commerce Co., Ltd. (Owner Number: 10057154)

Owner / Operator Contact Address

Room 111, Building 7, No. 96, Rd. Lixin 12, Xintang Town, Zengcheng District, Guangzhou, CN-GD 511300, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

male masturbation toy/sex toy kegel ball/sex toy prostate massager/sex toy anal plug/sex toy Realistic Dildo/sex toy massager/Electric Massager male masturbation cup/sex toy vibrator/sex toy Personal lubricant

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
FCE	Enema Kit	Gastroenterology, Urology	Class 1	876.5210	2022-02-22
KHA	Mask, Scavenging	Anesthesiology	Class 1	868.5590	2020-03-06
LKY	Device, External Penile Rigidity	Gastroenterology, Urology	Class 2	876.5020	2022-02-22
LYG	Massager, Therapeutic, Manual	Physical Medicine	Class 1	890.5660	2018-02-28
KMJ	Lubricant, Patient	General Hospital	Class 1	880.6375	2018-03-06
KXQ	Vibrator For Therapeutic Use, Genital	Obstetrics/Gynecology	Class 2	884.5960	2022-02-22

Official Correspondent

Dan Zhou

US Agent Details

Kai Li Email: likai323@hotmail.com Phone: (501) 7778490

Related Public Records

Same Entity

Guangzhou Zhongshu E-Commerce 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
K820587	Abco Dealers, Inc.	WET PACK LINE OF PRODUCTS	1982-03-26

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3014615175	K-MED CO., LTD.	Yangzhou Jiangsu, CN
3011919098	NINGBO JUST SOON INDUSTRIAL LIMITED	Ningbo Zhejiang, CN
1921846	Cardinal Health	Hazelwood, MO, US

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3014326210. Last updated year: 2026. Please use registration number 3014326210 when referencing this establishment in official correspondence.