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Data / Medical devices / Intervertebral Fusion Device With Bone Graft, Lumbar / Germany

FDA-registered makers of Intervertebral Fusion Device With Bone Graft, Lumbar in Germany: 24 establishments

24 establishments in Germany are registered with the FDA to make Intervertebral Fusion Device With Bone Graft, Lumbar (product code MAX). 9 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
Intervertebral Fusion Device With Bone Graft, Lumbar
Product code
MAX
Country
Germany

Makers of Intervertebral Fusion Device With Bone Graft, Lumbar in Germany

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Medtronic Sofamor Danek Deggendorf GMBHDEGGENDORF Bavaria, GermanyManufacturer22September 6, 2024100api.fda.gov
Signus Medizintechnik GMBHALZENAU Bavaria, GermanyComplaint file establishment, Exporter to the US, Manufacturer, Specification developer7September 11, 2024000api.fda.gov
Eit Emerging Implant Technologies GMBHWurmlingen Baden-Wurttemberg, GermanyContract manufacturer, Specification developer5July 15, 2020000api.fda.gov
Silony Medical GMBHLeinfelden-Echterdingen Baden-Wurttemberg, GermanyComplaint file establishment, Specification developer5July 18, 2019000api.fda.gov
Aesculap AGTUTTLINGEN, DONAU Baden-Wurttemberg, GermanyManufacturer3August 13, 2015000api.fda.gov
Ngmedical GMBHNonnweiler Saarland, GermanyManufacturer3April 30, 2026000api.fda.gov
Joimax GMBHKARLSRUHE Baden-Wurttemberg, GermanyExporter to the US, Manufacturer2September 1, 2021000api.fda.gov
Ulrich GMBH & Co. KGULM Baden-Wurttemberg, GermanyManufacturer2June 21, 2013000api.fda.gov
BIEDERMANN MOTECH GMBH & Co. KGVS-SCHWENNINGEN Baden-Wurttemberg, GermanyManufacturer, Specification developer1June 2, 2017000api.fda.gov
Ackermann Instrumente GMBHRIETHEIM, WEILHEIM Baden-Wurttemberg, GermanyManufacturer0000api.fda.gov
Christian Diener GMBHTUTTLINGEN Baden-Wurttemberg, GermanyContract manufacturer0000api.fda.gov
Erchinger AGTUTTLINGEN Baden-Wurttemberg, GermanyContract manufacturer0000api.fda.gov
Eurofins Inpac Medizintechnik GMBHBirkenfeld Baden-Wurttemberg, GermanyContract manufacturer0000api.fda.gov
Eurofins STERIPAC GMBHCalw-Altburg Baden-Wurttemberg, GermanyContract manufacturer0000api.fda.gov
Friedrich Daniels GMBHSOLINGEN North Rhine-Westphalia, GermanyContract manufacturer0000api.fda.gov
Gebr. Brasseler GMBH & Co. KGLEMGO North Rhine-Westphalia, GermanyContract manufacturer0000api.fda.gov
Hipp Medical AGRenquishausen Baden-Wurttemberg, GermanyContract manufacturer0000api.fda.gov
Jabil Tuttlingen Manufacturing GmbHTuttlingen Baden-Wurttemberg, GermanyContract manufacturer0000api.fda.gov
Medcare Solutions GMBHEmmingen Baden-Wurttemberg, GermanyContract manufacturer0000api.fda.gov
Procon Medizintechnik GMBHAlzenau Bavaria, GermanyContract manufacturer0000api.fda.gov
Ptumedical GMBHSpaichingen Baden-Wurttemberg, GermanyContract manufacturer0000api.fda.gov
Puracon GMBHRosenheim Bavaria, GermanyContract manufacturer0000api.fda.gov
ProCon Implants GmbHTuttlingen Baden-Wurttemberg, GermanyContract manufacturer0000api.fda.gov
Tontarra Medizintechnik GMBHWURMLINGEN Baden-Wurttemberg, GermanyContract manufacturer0000api.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.