WENZHOU KANGSHUN MEDICAL DEVICES CO.,LTD.

FDA Device Registration & Listing · Wenzhou City Zhejiang, CN · Registration 3009154535

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
3009154535
FEI Number
3009154535
Entity Name
WENZHOU KANGSHUN MEDICAL DEVICES CO.,LTD.
City/State/Country
Wenzhou City Zhejiang, CN
Establishment Address
No.706 Yanyun Road,Lingkun Street,Oujiangkou Industrial Cluster District, Wenzhou City Zhejiang 325011, CN
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Wenzhou Kangshun Medical Devices Co.,Ltd. (Owner Number: 10089633)
Owner / Operator Contact Address
No.706 Yanyun Road,Lingkun Street,Oujiangkou Industrial Cluster District, Wenzhou City, CN-ZJ 325011, CN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K230859
PMA Number
N/A

All Registered Proprietary Names

,Aneroid Sphygmomanometer with stethoscope stethoscope Stethoscope Model:ks-2035,ks-2045,ks-2026,ks-2015,ks-2036,Aneroid Sphygmomanometer,Model:Ks-2201,ks-2021 hammer Aneroid Sphygmomanometer,Model:Ks-1222,Ks-1621,Ks-3201,Ks-2201,Ks-2203 ANEROID SPHYGMOMANOMETER Blood Pressure Cuff Aneroid Sphygmomanometer,Aneroid Sphygmomanometer With Stethoscope

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
LDE Stethoscope, Manual Cardiovascular Class 1 870.1875 2023-12-24
FZY Hammer, Surgical General, Plastic Surgery Class 1 878.4800 2025-03-20
DXQ Blood Pressure Cuff Cardiovascular Class 2 870.1120 2023-12-23
LDE Stethoscope, Manual Cardiovascular Class 1 870.1875 2023-12-23

Official Correspondent

Sheng Guang Wu

US Agent Details

Weian Huang Business: JOYSUN USA LLC Email: weian@isosh.com Phone: (949) 4624543

Related Public Records

Same Entity

Wenzhou Kangshun Medical Devices 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
K831001 Frontier Products UNICUFF-BLOOD PRESSURE CUFF 1983-07-28
K253089 Shenzhen Best Electronics Co., Ltd. NIBP Cuff (BCS-112, BCS-212, BCS-312, BCS-412, BCS-512, BCS-612, BCS-712, BCS-122, BCS-222, BCS-322, BCS-422, BCS-522, BCS-622, BCS-722, BCD-112, BCD-212, BCD-312, BCD-412, BCD-512, BCD-612, BCD-712, BCD-122, BCD-222, BCD-322, BCD-422, BCD-522, BCD-622, BCD-722) 2026-02-13
K972301 Rudolf Riester GmbH & Co. KG BIG BEN SQUARE, BIG BEN ROUND 1997-09-17

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3009154535. Last updated year: 2026. Please use registration number 3009154535 when referencing this establishment in official correspondence.
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