Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3015134755

FEI Number

3015134755

Entity Name

TAIZHOU HONOD MEDICAL CO.,LTD

City/State/Country

Taizhou Zhejiang, CN

Establishment Address

Room 301,Unit 1,Building 10,Weixing Phtoelectric Industrial Park,Datian Street Linhai City, Taizhou Zhejiang 317004, CN

Establishment Type(s)

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

Owner / Operator

TAIZHOU HONOD MEDICAL CO.,LTD (Owner Number: 10084231)

Owner / Operator Contact Address

Room 601,Building 19,Zhedong Leisure and furniture City,Datian Street,Linhai City,Zhejiang,317004, Taizhou, CN-ZJ 317004, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Honod Specimen containers Container, Specimen, Sterile Recloseable Bags CURETTE, EAR Honod vaginal speculum Speculum,vaginal, nonmetal SPECULUM, ENT

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
NNI	Container, Specimen, Non-Sterile	Pathology	Class 1	864.3250	2022-01-28
FMH	Container, Specimen, Sterile	Pathology	Class 1	864.3250	2023-03-27
JYG	Curette, Ear	Ear, Nose, Throat	Class 1	874.4420	2024-10-21
KYW	Container, Liquid Medication, Graduated	General Hospital	Class 1	880.6430	2022-01-27
HIB	Speculum, Vaginal, Nonmetal	Obstetrics/Gynecology	Class 2	884.4530	2022-01-27
EPY	Speculum, Ent	General, Plastic Surgery	Class 1	878.1800	2024-10-21

Official Correspondent

Henry Zhang

US Agent Details

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

Related Public Records

Same Entity

TAIZHOU HONOD MEDICAL 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
K834189	Imm Enterprises , Ltd.	JAKOBI SURG. INSTRUMENTS #7 44/47	1984-03-06

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3015134755. Last updated year: 2026. Please use registration number 3015134755 when referencing this establishment in official correspondence.