Data / Medical devices / Orthosis, Spinal Pedicle Fixation / Germany

FDA-registered makers of Orthosis, Spinal Pedicle Fixation in Germany: 20 establishments

Name: FDA-registered makers of Orthosis, Spinal Pedicle Fixation in Germany
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

20 establishments in Germany are registered with the FDA to make Orthosis, Spinal Pedicle Fixation (product code MNI). 2 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: Orthosis, Spinal Pedicle Fixation
Product code: MNI
Country: Germany

Makers of Orthosis, Spinal Pedicle Fixation in Germany

Maker	Location	Role	510(k) clearances	Latest clearance	Source
Aesculap AG	TUTTLINGEN, DONAU Baden-Wurttemberg, Germany	Complaint file establishment, Manufacturer	5	February 3, 2006	api.fda.gov
Signus Medizintechnik GMBH	ALZENAU Bavaria, Germany	Complaint file establishment, Exporter to the US, Manufacturer, Specification developer	1	October 22, 2003	api.fda.gov
BIEDERMANN MOTECH GMBH & Co. KG	VS-SCHWENNINGEN Baden-Wurttemberg, Germany	Manufacturer, Specification developer	0		api.fda.gov
Christian Diener GMBH	TUTTLINGEN Baden-Wurttemberg, Germany	Contract manufacturer	0		api.fda.gov
Erchinger AG	TUTTLINGEN Baden-Wurttemberg, Germany	Contract manufacturer	0		api.fda.gov
Eurofins STERIPAC GMBH	Calw-Altburg Baden-Wurttemberg, Germany	Contract manufacturer	0		api.fda.gov
Friedrich Daniels GMBH	SOLINGEN North Rhine-Westphalia, Germany	Contract manufacturer	0		api.fda.gov
HG Medical GmbH	Raisting Bavaria, Germany	Contract manufacturer	0		api.fda.gov
Hipp Medical AG	Renquishausen Baden-Wurttemberg, Germany	Contract manufacturer	0		api.fda.gov
JAKUTEC MEDIZINTECHNIK GMBH & Co. KG	LIPTINGEN Baden-Wurttemberg, Germany	Contract manufacturer	0		api.fda.gov
Joimax GMBH	KARLSRUHE Baden-Wurttemberg, Germany	Manufacturer, Repackager or relabeler, Specification developer	0		api.fda.gov
Medcare Solutions GMBH	Emmingen Baden-Wurttemberg, Germany	Contract manufacturer	0		api.fda.gov
MEDITEC SOURCE GmbH & Co. KG	Tuttlingen-Nendingen Baden-Wurttemberg, Germany	Contract manufacturer	0		api.fda.gov
Medtronic Sofamor Danek Deggendorf GMBH	DEGGENDORF Bavaria, Germany	Manufacturer	0		api.fda.gov
Procon Medizintechnik GMBH	Alzenau Bavaria, Germany	Contract manufacturer	0		api.fda.gov
Puracon GMBH	Rosenheim Bavaria, Germany	Contract manufacturer	0		api.fda.gov
Rudolf Storz GMBH	EMMINGEN Baden-Wurttemberg, Germany	Contract manufacturer	0		api.fda.gov
Ulrich GMBH & Co. KG	ULM Baden-Wurttemberg, Germany	Manufacturer	0		api.fda.gov
W+S Solutions GMBH	Tuttlingen Baden-Wurttemberg, Germany	Contract manufacturer	0		api.fda.gov
Z-Medical GMBH & Co. KG	Tuttlingen Baden-Wurttemberg, Germany	Manufacturer	0		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.