SHENZHEN CANWIN HEALTH PRODUCTS CO., LTD

FDA Device Registration & Listing · Shenzhen Guangdong, CN · Registration 3012110942

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
3012110942
FEI Number
3012110942
Entity Name
SHENZHEN CANWIN HEALTH PRODUCTS CO., LTD
City/State/Country
Shenzhen Guangdong, CN
Establishment Address
No.9, GuiRi Road , Guanlan Community,Longhua District ,, Shenzhen Guangdong 518110, CN
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Shenzhen CanWin Health Products Co., Ltd (Owner Number: 10089399)
Owner / Operator Contact Address
No.9, GuiRi Road , Guanlan Community,Longhua District ,, Shenzhen, CN-GD 518110, CN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Lubricant, patient MASSAGER, THERAPEUTIC, MANUAL MASK, SCAVENGING Massager, therapeutic, electric Vibrator for therapeutic use, genital

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KMJ Lubricant, Patient General Hospital Class 1 880.6375 2025-12-16
LYG Massager, Therapeutic, Manual Physical Medicine Class 1 890.5660 2025-12-16
KHA Mask, Scavenging Anesthesiology Class 1 868.5590 2025-12-16
ISA Massager, Therapeutic, Electric Physical Medicine Class 1 890.5660 2025-12-16
KXQ Vibrator For Therapeutic Use, Genital Obstetrics/Gynecology Class 2 884.5960 2025-12-16
LKY Device, External Penile Rigidity Gastroenterology, Urology Class 2 876.5020 2023-12-05

Official Correspondent

Kechuan Zheng

US Agent Details

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

Related Public Records

Same Entity

Shenzhen CanWin Health Products 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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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3012110942. Last updated year: 2026. Please use registration number 3012110942 when referencing this establishment in official correspondence.
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