DIPPED PRODUCTS (THAILAND) LTD

FDA Device Registration & Listing · AMPHUR KHUN NIENG Songkhla, TH · Registration 3005024094

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
3005024094
FEI Number
3005024094
Entity Name
DIPPED PRODUCTS (THAILAND) LTD
City/State/Country
AMPHUR KHUN NIENG Songkhla, TH
Establishment Address
82/2 MOO 9, TUMBON RATTAPUM, AMPHUR KHUN NIENG Songkhla 90220, TH
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
DIPPED PRODUCTS (THAILAND) LTD (Owner Number: 9069755)
Owner / Operator Contact Address
82/2 MOO 9, TUMBON RATTAPUM, AMPHUR KHUAN NIENG, SONGKHLA, TH-NOTA 90220, TH
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

SW N20036 Exam GLOVES PALM PRO PALM PRO PREMIUM PALM-PRO POWDER FREE NITRILE EXAMINATION GLOVES PALM PRO NITRILE POWDER FREE EXAMINATION GLOVES

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 2022-11-13
LYY Latex Patient Examination Glove General Hospital Class 1 880.6250 2007-12-14
LZA Polymer Patient Examination Glove General Hospital Class 1 880.6250 2012-08-03
LZC Medical Glove, Specialty General Hospital Class 1 880.6250 2017-09-26
LZA Polymer Patient Examination Glove General Hospital Class 1 880.6250 2017-09-26
LZA Polymer Patient Examination Glove General Hospital Class 1 880.6250 2015-03-16

Official Correspondent

Prabhath Mendis

US Agent Details

Yong Sun Business: Emergo Global Representation LLC Email: USAgent@ul.com Phone: (512) 3279997

Related Public Records

Same Entity

DIPPED PRODUCTS (THAILAND) 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

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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 3005024094. Last updated year: 2026. Please use registration number 3005024094 when referencing this establishment in official correspondence.
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