Menasha Packaging LLC

FDA Device Registration & Listing · Alsip, IL, US · Registration 3020305857

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
3020305857
FEI Number
3020305857
Entity Name
Menasha Packaging LLC
City/State/Country
Alsip, IL, US
Establishment Address
11671 South Central ave, Alsip, IL 60803, US
Establishment Type(s)
Repack or Relabel Medical Device
Owner / Operator
Menasha Packaging Co. LLC (Owner Number: 10045291)
Owner / Operator Contact Address
1645 Bergstrom Road, Neenah, WI 54956, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
HGX Pump, Breast, Powered Obstetrics/Gynecology Class 2 884.5160 2023-01-05

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Menasha Packaging Co. LLC
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Other Registrations for Same Entity

Registration Number Establishment Name Location
3014128751 MENASHA Packaging Company, LLC Dallas, TX, US
3021035729 Menasha Packaging Company, LLC Lebanon, PA, US
3003896222 Menasha Packaging Company ,LLC EDISON, NJ, US
3010749695 Menasha Packaging Compnay Edwardsville, IL, US
3004764532 Menasha Packaging Company Newville, PA, US

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K190465 Hygeia II Medical Group, Inc. Evolve Breast Pump 2019-10-18
K021739 Limerick, Inc. LIMERICK POWERED ELECTRIC BREAST PUMP MODEL 1002 2003-01-10

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3020305857. Last updated year: 2026. Please use registration number 3020305857 when referencing this establishment in official correspondence.
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