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Data / Medical devices / Endoscopic Irrigation/Suction System / Germany

FDA-registered makers of Endoscopic Irrigation/Suction System in Germany: 6 establishments

6 establishments in Germany are registered with the FDA to make Endoscopic Irrigation/Suction System (product code OCX). 3 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
Endoscopic Irrigation/Suction System
Product code
OCX
Country
Germany

Makers of Endoscopic Irrigation/Suction System in Germany

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Karl Storz Se & Co KGTUTTLINGEN Baden-Wurttemberg, GermanySpecification developer2April 28, 2004000api.fda.gov
Erbe Elektromedizin GMBHTUEBINGEN Baden-Wurttemberg, GermanySpecification developer1December 23, 2010000api.fda.gov
Ovesco Endoscopy AGTuebingen Baden-Wurttemberg, GermanyComplaint file establishment, Manufacturer1May 22, 2025000api.fda.gov
Eurofins STERIPAC GMBHCalw-Altburg Baden-Wurttemberg, GermanyContract manufacturer0000api.fda.gov
Karl Storz Se & Co. KGTUTTLINGEN Baden-Wurttemberg, GermanyContract manufacturer0000api.fda.gov
Karl Storz Se & Co. KGNEUHAUSEN OBECK 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.