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Data / Medical devices / Accessories, Cleaning Brushes, For Endoscope / Germany

FDA-registered makers of Accessories, Cleaning Brushes, For Endoscope in Germany: 21 establishments

21 establishments in Germany are registered with the FDA to make Accessories, Cleaning Brushes, For Endoscope (product code MNL). 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
Accessories, Cleaning Brushes, For Endoscope
Product code
MNL
Country
Germany

Makers of Accessories, Cleaning Brushes, For Endoscope in Germany

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Almikro GMBH & Co. KGBad Krozingen Baden-Wurttemberg, GermanyContract manufacturer0000api.fda.gov
Axel Gentner GMBHTuttlingen Baden-Wurttemberg, GermanyContract manufacturer0000api.fda.gov
Eberle GmbH & Co. KGWURMBERG Baden-Wurttemberg, GermanyContract manufacturer0000api.fda.gov
H.+H. Maslanka Chirurgische Instrumente GmbHTuttlingen Baden-Wurttemberg, GermanyContract manufacturer0000api.fda.gov
Hebumedical GMBHTUTTLINGEN Baden-Wurttemberg, GermanyContract manufacturer, Manufacturer0000api.fda.gov
Heinrich Medizintechnik GMBHStuttgart Baden-Wurttemberg, GermanyManufacturer0000api.fda.gov
Helmut Zepf Medizintechnik GMBHSEITINGEN Baden-Wurttemberg, GermanyManufacturer0000api.fda.gov
Hermann Medizintechnik GMBHFRIDINGEN Baden-Wurttemberg, GermanyContract manufacturer0000api.fda.gov
HGR Instrumente GMBHTUTTLINGEN Baden-Wurttemberg, GermanyContract manufacturer0000api.fda.gov
Hoogland Spine Products GmbHUnterfoehring Munich Bavaria, GermanyExporter to the US, Specification developer0000api.fda.gov
Joimax GMBHKARLSRUHE Baden-Wurttemberg, GermanyExporter to the US, Manufacturer0000api.fda.gov
Karl Storz Se & Co KGTUTTLINGEN Baden-Wurttemberg, GermanySpecification developer0000api.fda.gov
Karl Storz Se & Co. KGTUTTLINGEN Baden-Wurttemberg, GermanyContract manufacturer0000api.fda.gov
Karl Storz Se & Co. KGTUTTLINGEN Baden-Wurttemberg, GermanyContract manufacturer, Repackager or relabeler0000api.fda.gov
Karl Storz Se & Co. KGNEUHAUSEN OBECK Baden-Wurttemberg, GermanyContract manufacturer0000api.fda.gov
Mattes Instrumente GMBHTuttlingen-Nendingen Baden-Wurttemberg, GermanyManufacturer, Repackager or relabeler0000api.fda.gov
Olympus Winter & Ibe GMBHHamburg, GermanyComplaint file establishment, Exporter to the US, Specification developer0000api.fda.gov
QUESTALPHA GmbH & Co. KGEschenburg Hesse, GermanyManufacturer0000api.fda.gov
Richard Wolf GMBHKNITTLINGEN Baden-Wurttemberg, GermanyManufacturer0000api.fda.gov
RZ Medizintechnik GMBHTUTTLINGEN Baden-Wurttemberg, GermanyContract manufacturer0000api.fda.gov
Saettele GMBH & Co. KGTodtnau 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.