SANREA HEALTHCARE PRODUCTS PVT LTD

FDA Device Registration & Listing · Palakkad Kerala, IN · Registration 3013530281

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
3013530281
FEI Number
3013530281
Entity Name
SANREA HEALTHCARE PRODUCTS PVT LTD
City/State/Country
Palakkad Kerala, IN
Establishment Address
Plot # P-56, Pearl Road, Kinfra Integrated Industrial & Textile Park, Kanjikode, Palakkad Kerala 678 621, IN
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
SANREA HEALTHCARE PRODUCTS PVT LTD (Owner Number: 10053578)
Owner / Operator Contact Address
Plot # P-56, Pearl Road, Kinfra Integrated Ind & Textile Park, Palakkkad, IN-KL 678 621, IN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Sterile Latex Examination Gloves Powderfree Dynarex GLOVTek SanCare Sterile Nitrile Examination Gloves Powderfree Sterile Latex Surgical Gloves Powderfree GLOVTek SanCare

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
LYY Latex Patient Examination Glove General Hospital Class 1 880.6250 2016-12-19
LZA Polymer Patient Examination Glove General Hospital Class 1 880.6250 2018-12-13
LZA Polymer Patient Examination Glove General Hospital Class 1 880.6250 2016-12-19
KGO Surgeon'S Gloves General, Plastic Surgery Class 1 878.4460 2016-12-19

Official Correspondent

No official correspondent registered.

US Agent Details

Manoj Zacharias Business: Liberty Management Group Ltd. Email: office@libertymanagement.us Phone: (630) 2702921

Related Public Records

Same Entity

SANREA HEALTHCARE PRODUCTS PVT 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
K894452 Kerala Rubber & Reclaims, Ltd. KRR GLOVE, PATIENT EXAMINATION GLOVES 1989-08-09
K891323 Li Wah-Hong Kong, Inc. LI WAH LATEX EXAMINATION GLOVES 1989-08-31
K891418 C & K Mfg. & Sales Co. LATEX EXAMINATION GLOVES, STYLE 510 LX 1989-06-22
K994255 Pt. Maja Agung Latexindo LATEX EXAMINATION GLOVES-PRE-POWDERED-STERILE 2000-02-07
K892946 Yeou-Fwu Rubber Industrial Co., Ltd. STERILE PATIENT EXAMINATION GLOVES 1989-08-10

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8040653 ARISTA LATINDO INDUSTRIAL, LTD. P.T. JAKARTA BARAT, ID
3002661124 ULINE, INC. Pleasant Prairie, WI, US
3019769825 HARTALEGA NGC SDN. BHD. (LOT 39496) Sepang Selangor, MY
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3013530281. Last updated year: 2026. Please use registration number 3013530281 when referencing this establishment in official correspondence.
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