MATANG MFG. SDN. BHD.

FDA Device Registration & Listing · MERLIMAU Melaka, MY · Registration 8041120

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
8041120
FEI Number
3003602484
Entity Name
MATANG MFG. SDN. BHD.
City/State/Country
MERLIMAU Melaka, MY
Establishment Address
LOT 10, KAWASAN PERINDUSTRIAN, SERKAM, MUKIM SERKAM, MERLIMAU Melaka 77300, MY
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer),Manufacture Medical Device
Owner / Operator
MATANG MFG. SDN. BHD. (Owner Number: 8041120)
Owner / Operator Contact Address
LOT 10, KAWASAN PERINDUSTRIAN, SERKAM, MUKIM SERKAM, MERLIMAU, MELAKA, MY-NOTA 77300, MY
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K032549
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 2013-01-25
LZC Medical Glove, Specialty General Hospital Class 1 880.6250 2013-01-25
LYY Latex Patient Examination Glove General Hospital Class 1 880.6250 2008-12-15
LYY Latex Patient Examination Glove General Hospital Class 1 880.6250 2007-12-08
LZA Polymer Patient Examination Glove General Hospital Class 1 880.6250 2013-01-25
LZA Polymer Patient Examination Glove General Hospital Class 1 880.6250 2007-12-08

Official Correspondent

No official correspondent registered.

US Agent Details

Jerry Leong Business: Mr Jerry Leong Email: jleong@medgluv.com Phone: (561) 2128885

Related Public Records

Same Entity

MATANG MFG. SDN. BHD.
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

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 8041120. Last updated year: 2026. Please use registration number 8041120 when referencing this establishment in official correspondence.
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