ZOUPURE MEDIC Co., Ltd.

FDA Device Registration & Listing · Ban Khai Rayong, TH · Registration 3023191174

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
3023191174
FEI Number
3023191174
Entity Name
ZOUPURE MEDIC Co., Ltd.
City/State/Country
Ban Khai Rayong, TH
Establishment Address
168 Moo 1, Nong Bua, Ban Khai Rayong 21120, TH
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Zoupure Medic Co., Ltd. (Owner Number: 10085422)
Owner / Operator Contact Address
168 Moo 1, Nong Bua, Ban Khai, TH-21 21120, TH
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

Zoupure Glove

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 2022-06-15

Official Correspondent

Kanjana Boonpun

US Agent Details

Da Shi Email: fdaagent@medicaldevice.org Phone: (716) 7906888

Related Public Records

Same Entity

Zoupure Medic 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
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 3023191174. Last updated year: 2026. Please use registration number 3023191174 when referencing this establishment in official correspondence.
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