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Data / Medical devices / United States / Menasha Packaging LLC

Menasha Packaging LLC: FDA-registered device maker in Alsip, IL, United States, 3 510(k) clearances

Menasha Packaging LLC is registered with the FDA (registration 3020305857) in Alsip, IL, United States. It lists 5 device types. The FDA files 3 510(k) clearances under its listings, the newest dated January 6, 2023. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
3020305857
Address
11671 South Central ave, Alsip, IL, United States, 60803
Owner or operator
Menasha Packaging Co. LLC (10045291)
Roles
Repackager or relabeler
First device listed
August 3, 2015
Registered through
2026

Devices it lists

510(k) clearances

The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.

Decided510(k) numberDeviceProduct codeDecisionApplicantSource
January 6, 2023K223749U by Kotex® Click® Unscented Menstrual TamponsHEBSubstantially EquivalentKimberly-Clark Corporationaccessdata.fda.gov
December 23, 2022K222726Smartpump 3.0 Double Electric Breast PumpHGXSubstantially EquivalentLansinoh Laboratoriesaccessdata.fda.gov
October 11, 2017K172118U by Kotex Click Unscented Menstrual TamponsHEBSubstantially EquivalentKimberly-Clark Corporationaccessdata.fda.gov

Compare with other makers

Updated January 6, 2023. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.