CROSS PROTECTION M SDN BHD

FDA Device Registration & Listing · Klang Selangor, MY · Registration 3008107579

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
3008107579
FEI Number
3008107579
Entity Name
CROSS PROTECTION M SDN BHD
City/State/Country
Klang Selangor, MY
Establishment Address
NO. 18, PERSIARAN ASTANA /KU 2, Bandar Bkt Raja,, Klang Selangor 41050, MY
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
CROSS PROTECTION M SDN BHD (Owner Number: 10036184)
Owner / Operator Contact Address
No 11, JLN PERINDUSTRIAN 5, BATU 5 1/2, OFF JLN HJ ABDUL MANAN, KLANG, MY-10 41050, MY
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Cross Protection Cross Protection Saliva Ejector Tip Cross Protection Saliva Ejector Cross Protection Cross Protection ResQ300 Plus Surgical Face Mask Cross Protection

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 2013-08-21
DYN Mouthpiece, Saliva Ejector Dental Class 1 872.6640 2011-04-21
LYY Latex Patient Examination Glove General Hospital Class 1 880.6250 2015-07-02
FXX Mask, Surgical General, Plastic Surgery Class 2 878.4040 2022-12-20
LYU Accessory, Surgical Apparel General, Plastic Surgery Class 1 878.4040 2014-11-08

Official Correspondent

No official correspondent registered.

US Agent Details

David Lennarz Business: Registrar Corp Email: david.lennarz@registrarcorp.com Phone: (757) 2240177

Related Public Records

Same Entity

CROSS PROTECTION M 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
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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1000266564 SRI TRANG GLOVES (THAILAND) PUBLIC COMPANY LIMITED. Hat Yai Songkhla, TH
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 3008107579. Last updated year: 2026. Please use registration number 3008107579 when referencing this establishment in official correspondence.
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