Data / Medical devices / Equipment, Laboratory, General Purpose, Labeled Or Promoted For A Specific Medical Use / Germany

FDA-registered makers of Equipment, Laboratory, General Purpose, Labeled Or Promoted For A Specific Medical Use in Germany: 15 establishments

Name: FDA-registered makers of Equipment, Laboratory, General Purpose, Labeled Or Promoted For A Specific Medical Use in Germany
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

15 establishments in Germany are registered with the FDA to make Equipment, Laboratory, General Purpose, Labeled Or Promoted For A Specific Medical Use (product code LXG). 0 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.

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Device: Equipment, Laboratory, General Purpose, Labeled Or Promoted For A Specific Medical Use
Product code: LXG
Country: Germany

Makers of Equipment, Laboratory, General Purpose, Labeled Or Promoted For A Specific Medical Use in Germany

Maker	Location	Role	Source
BALDA MEDICAL GmbH	Bad Oeynhausen North Rhine-Westphalia, Germany	Contract manufacturer	api.fda.gov
Bort GmbH	WEINSTADT-BENZACH Baden-Wurttemberg, Germany	Manufacturer	api.fda.gov
Eppendorf Se	Hamburg, Germany	Contract manufacturer	api.fda.gov
Euroimmun Medizinische Labordiagnostika AG	Luebeck Schleswig-Holstein, Germany	Manufacturer	api.fda.gov
EUROIMMUN Medizinische Labordiagnostika AG	Dassow Mecklenburg-Western Pomerania, Germany	Manufacturer	api.fda.gov
Eppendorf Polymere GmbH	Oldenburg Schleswig-Holstein, Germany	Contract manufacturer	api.fda.gov
Human Med AG	SCHWERIN Mecklenburg-Western Pomerania, Germany	Manufacturer	api.fda.gov
Ibl International GMBH	Hamburg, Germany	Exporter to the US, Manufacturer, Repackager or relabeler	api.fda.gov
Medite Medical GMBH	Burgdorf Lower Saxony, Germany	Manufacturer	api.fda.gov
Microfluidic Chipshop GMBH	Jena Thuringia, Germany	Contract manufacturer, Manufacturer	api.fda.gov
PFM Medical GmbH	COLOGNE North Rhine-Westphalia, Germany	Complaint file establishment, Manufacturer	api.fda.gov
Roche Diagnostics GMBH	MANNHEIM Baden-Wurttemberg, Germany	Exporter to the US, Manufacturer, Specification developer	api.fda.gov
Rudolf Storz GMBH	EMMINGEN Baden-Wurttemberg, Germany	Manufacturer	api.fda.gov
Roche Diagnostics Automation Solutions GmbH	Ludwigsburg Baden-Wurttemberg, Germany	Manufacturer	api.fda.gov
Sarstedt AG & Co. KG	NUMBRECHT North Rhine-Westphalia, Germany	Manufacturer	api.fda.gov

Updated November 2, 2026. 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.