Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3017114229

FEI Number

3017114229

Entity Name

MEDTECS MSEZ CORP., LTD.

City/State/Country

Krong Bavet Svay Rieng, KH

Establishment Address

Manhattan SEZ, National Road #1, Sangkat Baty, Krong Bavet Svay Rieng 120407, KH

Establishment Type(s)

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

Owner / Operator

MEDTECS MSEZ CORP., LTD. (Owner Number: 10092237)

Owner / Operator Contact Address

Manhattan SEZ, National Road #1, Sangkat Baty, Krong Bavet, KH-20 120407, KH

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K070861

PMA Number

N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
LZA	Polymer Patient Examination Glove	General Hospital	Class 1	880.6250	2025-06-13
OPJ	Medical Gloves With Chemotherapy Labeling Claims - Test For Use With Chemotherapy Drugs	General Hospital	Class 1	880.6250	2024-12-16
QDO	Fentanyl And Other Opioid Protection Glove	General Hospital	Class 1	880.6250	2024-12-16
LZC	Medical Glove, Specialty	General Hospital	Class 1	880.6250	2024-12-16
LZA	Polymer Patient Examination Glove	General Hospital	Class 1	880.6250	2024-12-16
LZC	Medical Glove, Specialty	General Hospital	Class 1	880.6250	2025-06-17
LZA	Polymer Patient Examination Glove	General Hospital	Class 1	880.6250	2025-06-17
LZA	Polymer Patient Examination Glove	General Hospital	Class 1	880.6250	2025-01-02

Official Correspondent

Tina Jia

US Agent Details

You You Email: fdaregistration@csrepresent.com Phone: (909) 5901611

Related Public Records

Same Entity

MEDTECS MSEZ CORP., 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
K212801	Hong Seng Gloves Sdn Bhd	Powder free nitrile examination glove- black, non sterile	2022-01-09
K260806	Vista Industries,, LLC	Nitrile Disposable Examination Gloves	2026-06-03
K011593	Ansell Healthcare Products, Inc.	MICRO-TOUCH NITRILE POWDER FREE SYNTHETIC MEDICAL EXAMINATION GLOVES, COLOR BLUE NON-STERILE	2001-06-21
K981039	Sri Johani Sdn. Bhd.	POWDERFREE GREEN NITRILE EXAMINATION GLOVES (POLYMER COATED)	1998-04-21
K101595	Better Care Plastic Technology Cp., Ltd.	POWDER FREE NITRILE PATIENT EXAMINATION GLOVES, BLUE	2010-08-06

Similar Registrations

Registration Number	Establishment Name	Location
3030671502	GUANGDONG VYIMED CO., LTD.	Qingyuan Guangdong, CN
9610406	ANSELL (THAILAND) LTD.	THAILAND Krung Thep Maha Nakhon, TH
3026062711	RMKH GLOVE (CAMBODIA) CO., LTD.	Bavet City Svay Rieng, KH
3043739177	US Paper Mill LLC	Chillicothe, OH, US
3042765418	VITAL EDGE INSTRUMENTS LLC	Leesburg, VA, US

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3017114229. Last updated year: 2026. Please use registration number 3017114229 when referencing this establishment in official correspondence.