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Data / Medical devices / United States / MENASHA Packaging Company, LLC

MENASHA Packaging Company, LLC: FDA-registered device maker in Dallas, TX, United States, 2 510(k) clearances

MENASHA Packaging Company, LLC is registered with the FDA (registration 3014128751) in Dallas, TX, United States. It lists 4 device types. The FDA files 2 510(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
3014128751
FEI number
3012428604
Address
4808 Mountain Creek Pkwy, Dallas, TX, United States, 75236
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
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.