ZHEJIANG HONSUN MEDICAL TECHNOLOGY CO., LTD.

FDA Device Registration & Listing · Wenzhou City Zhejiang, CN · Registration 3017805218

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
3017805218
FEI Number
3017805218
Entity Name
ZHEJIANG HONSUN MEDICAL TECHNOLOGY CO., LTD.
City/State/Country
Wenzhou City Zhejiang, CN
Establishment Address
Floor 2 and Floor3, Building 8 of Art and Crafts Park, Beiao Village, Sanjiang Street, Yongjia County, Wenzhou City Zhejiang 325100, CN
Establishment Type(s)
Export Device to the United States But Perform No Other Operation on Device,Manufacture Medical Device
Owner / Operator
ZHEJIANG HONSUN MEDICAL TECHNOLOGY CO., LTD. (Owner Number: 10091651)
Owner / Operator Contact Address
Floor 2 & Floor3, Building 8 of Art & Crafts Park, Beiao Village, Sanjiang Street, Yongjia County, Wenzhou City, CN-ZJ 325100, CN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Manual Stethoscope Hammer Otoscope Tourniquet Jeashia Ophthalmoscope, Ophthalmoscope

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
LDE Stethoscope, Manual Cardiovascular Class 1 870.1875 2026-01-19
GWZ Percussor Neurology Class 1 882.1700 2026-01-14
ERA Otoscope Ear, Nose, Throat Class 1 874.4770 2026-01-14
GAX Tourniquet, Nonpneumatic General, Plastic Surgery Class 1 878.5900 2026-01-14
HLJ Ophthalmoscope, Battery-Powered Ophthalmic Class 2 886.1570 2024-10-22

Official Correspondent

Jinshan Wang

US Agent Details

Leeyeo Kee Business: Regrek LLC Email: regrek.cs@hotmail.com Phone: (302) 6089028

Related Public Records

Same Entity

ZHEJIANG HONSUN MEDICAL TECHNOLOGY 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
K932506 Rudolf Riester GmbH & Co. KG RI-SCOPE (S) 1993-10-08

Similar Registrations

Registration Number Establishment Name Location
3009154535 WENZHOU KANGSHUN MEDICAL DEVICES CO.,LTD. Wenzhou City Zhejiang, CN
3003897648 MOREPEN LABORATORIES LIMITED Baddi, Solan Himachal Pradesh, IN
3031192529 Zhejiang LuDe Technology Development Co., Ltd. Wenzhou Zhejiang, CN
3042481106 SMART HEALTH LLC Owings Mills, MD, US
3025413691 BESTREAT SAFETY & FIRST AID SOLUTION CO., LTD Wuhan Hubei, CN
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3017805218. Last updated year: 2026. Please use registration number 3017805218 when referencing this establishment in official correspondence.
Legal Disclaimer: AvaSpecs is not affiliated with the FDA or any government agency and does not provide medical, legal, regulatory, safety, approval, clearance, effectiveness, endorsement, or compliance advice. This index page is built using public record archives and does not represent an official regulatory determination.
Account Required Full available specs will require a free AvaSpecs account.