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Data / Medical devices / Germany / Medizin-Mechanik - Nord GMBH

Medizin-Mechanik - Nord GMBH: FDA-registered device maker in Kiel Schleswig-Holstein, Germany, 1 510(k) clearance

Medizin-Mechanik - Nord GMBH is registered with the FDA (registration 3010411051) in Kiel Schleswig-Holstein, Germany. It lists 2 device types. The FDA files 1 510(k) clearance under its listings, the newest dated October 10, 2008. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
3010411051
Address
Russeer Weg 54a, Kiel Schleswig-Holstein, Germany, 24111
Owner or operator
Medizin-Mechanik - Nord GmbH (10043973)
Roles
Manufacturer
First device listed
April 12, 2013
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
October 10, 2008K082018T2 FLEXIBLE NAILHSBSubstantially EquivalentHowmedica Osteonics Corp.accessdata.fda.gov

Compare with other makers

Updated October 10, 2008. 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.