Data / Medical devices / France / Rhenus Logistics Gretz

Rhenus Logistics Gretz: FDA-registered device maker in Chatres Seine-et-Marne, France, 1 510(k) clearance

Rhenus Logistics Gretz is registered with the FDA (registration 3030794592) in Chatres Seine-et-Marne, France. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated August 28, 2024. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number

3030794592

Address

Batiment 6 ZAC du Val BREON, Av Louis Renault, Chatres Seine-et-Marne, France, 77610

Owner or operator

Rhenus Logistics Gretz (10092565)

Roles

Exporter to the US, Repackager or relabeler

First device listed

January 22, 2025

Registered through

2026

Brand names listed

Chronos

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.

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Updated August 28, 2024. 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.