American Pride Paper & Plastic LLC.

FDA Device Registration & Listing · Lakewood, NJ, US · Registration 3011665414

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
3011665414
FEI Number
3011665414
Entity Name
American Pride Paper & Plastic LLC.
City/State/Country
Lakewood, NJ, US
Establishment Address
600 james street, Lakewood, NJ 08701, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
cw international sales LLC. (Owner Number: 10030142)
Owner / Operator Contact Address
600 james street, Lakewood, NJ 08701, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
K052502
PMA Number
N/A

All Registered Proprietary Names

Safe Gaurd

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 2025-06-04

Official Correspondent

Nisson Kugler

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

cw international sales LLC.
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 3011665414. Last updated year: 2026. Please use registration number 3011665414 when referencing this establishment in official correspondence.
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