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Data / Medical devices / Sterilization Wrap Containers, Trays, Cassettes & Other Accessories / Germany

FDA-registered makers of Sterilization Wrap Containers, Trays, Cassettes & Other Accessories in Germany: 21 establishments

21 establishments in Germany are registered with the FDA to make Sterilization Wrap Containers, Trays, Cassettes & Other Accessories (product code KCT). 13 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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Get makers of this device in GermanyWatch these makers
Device
Sterilization Wrap Containers, Trays, Cassettes & Other Accessories
Product code
KCT
Country
Germany

Makers of Sterilization Wrap Containers, Trays, Cassettes & Other Accessories in Germany

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Aesculap AGTUTTLINGEN, DONAU Baden-Wurttemberg, GermanyComplaint file establishment, Contract manufacturer, Manufacturer9March 27, 2020000api.fda.gov
Olympus Winter & Ibe GMBHHamburg, GermanyComplaint file establishment, Exporter to the US, Specification developer4September 15, 2021000api.fda.gov
Sirona Dental Systems GmbHBensheim Hesse, GermanySpecification developer4September 4, 2026000api.fda.gov
Karl Storz Se & Co KGTUTTLINGEN Baden-Wurttemberg, GermanySpecification developer2May 7, 2021000api.fda.gov
Argon Medical Productions & Vertriebs Gesellschaft MBH & Co.Bingen am Rhein Rhineland-Palatinate, GermanyManufacturer1December 20, 2016000api.fda.gov
Bego Implant Systems GMBH & Co. KGBremen, GermanyManufacturer1February 18, 2021000api.fda.gov
Ermis MedTechTUTTLINGEN Baden-Wurttemberg, GermanyManufacturer1July 5, 2013000api.fda.gov
Gebr. Schwarz GmbHRottweil Baden-Wurttemberg, GermanyContract manufacturer, Repackager or relabeler1December 20, 1994000api.fda.gov
Karl Storz Se & Co. KGTUTTLINGEN Baden-Wurttemberg, GermanyContract manufacturer, Specification developer1July 6, 2021000api.fda.gov
Medicon, E.G.TUTTLINGEN Baden-Wurttemberg, GermanyManufacturer1August 2, 2002000api.fda.gov
Medtronic Sofamor Danek Deggendorf GMBHDEGGENDORF Bavaria, GermanyManufacturer1October 15, 2019000api.fda.gov
Richard Wolf GMBHKNITTLINGEN Baden-Wurttemberg, GermanyManufacturer1June 3, 2024000api.fda.gov
Ustomed Instrumente GMBH & Co. KGTuttlingen Baden-Wurttemberg, GermanyContract manufacturer, Repackager or relabeler1July 5, 2013000api.fda.gov
Dentsply Implants Manufacturing GmbHHanau Hesse, GermanyContract manufacturer0000api.fda.gov
Hupfer Metallwerke GMBH & Co. KGCoesfeld North Rhine-Westphalia, GermanyContract manufacturer0000api.fda.gov
Hipp Medical AGRenquishausen Baden-Wurttemberg, GermanyContract manufacturer0000api.fda.gov
Inkutec GMBHBarsbüttel Schleswig-Holstein, GermanyContract manufacturer0000api.fda.gov
Intuitive Surgical Optics GmbHFreiburg Baden-Wurttemberg, GermanyManufacturer0000api.fda.gov
Karl Storz Se & Co. KGNEUHAUSEN OBECK Baden-Wurttemberg, GermanyContract manufacturer0000api.fda.gov
Rudolf Storz GMBHEMMINGEN Baden-Wurttemberg, GermanyContract manufacturer0000api.fda.gov
RZ Medizintechnik GMBHTUTTLINGEN 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.