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Data / Medical devices / Poland / Cordis Logistics SP. Z O.O.

Cordis Logistics SP. Z O.O.: FDA-registered device maker in Radomsko Lodzkie, Poland, 1 510(k) clearance

Cordis Logistics SP. Z O.O. is registered with the FDA (registration 3038282948) in Radomsko Lodzkie, Poland. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated December 19, 2012. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
3038282948
Address
ul. Sucharskiego 49, Radomsko Lodzkie, Poland, 97-500
Owner or operator
Cordis Logistics Sp. z o.o. (10093331)
Roles
Exporter to the US, Foreign private label distributor, Repackager or relabeler
First device listed
April 30, 2025
Registered through
2026
Brand names listed
Cordis

Devices it lists

DeviceProduct codeClassRoleSource
Tampon, Menstrual, UnscentedHEB2Exporter to the US, Foreign private label distributor, Repackager or relabeleraccessdata.fda.gov

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
December 19, 2012K122603ONTEX AND OTHER PROPRIETARY NAMESHEBSubstantially EquivalentOntex Bvbaaccessdata.fda.gov

Compare with other makers

Updated December 19, 2012. 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.