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Data / Medical devices / Hysteroscope (And Accessories) / Germany

FDA-registered makers of Hysteroscope (And Accessories) in Germany: 22 establishments

22 establishments in Germany are registered with the FDA to make Hysteroscope (And Accessories) (product code HIH). 9 have a 510(k) clearance or PMA approval on file and 1 has a recall event. FDA data exported November 2, 2026.

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Device
Hysteroscope (And Accessories)
Product code
HIH
Country
Germany

Makers of Hysteroscope (And Accessories) in Germany

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Karl Storz Se & Co KGTUTTLINGEN Baden-Wurttemberg, GermanySpecification developer13September 25, 2026000api.fda.gov
Olympus Winter & Ibe GMBHHamburg, GermanyComplaint file establishment, Exporter to the US, Manufacturer, Specification developer12December 22, 2021000api.fda.gov
Richard Wolf GMBHKNITTLINGEN Baden-Wurttemberg, GermanyManufacturer4December 23, 2003000api.fda.gov
Tekno Medical Optik-Chirurgie GMBHTUTTLINGEN-Nendingen Baden-Wurttemberg, GermanyManufacturer, Repackager or relabeler3June 8, 2018000api.fda.gov
Gimmi GMBHTUTTLINGEN Baden-Wurttemberg, GermanyManufacturer, Repackager or relabeler2June 8, 2018000api.fda.gov
Henke-Sass Wolf, GMBH.TUTTLINGEN Baden-Wurttemberg, GermanyContract manufacturer, Manufacturer, Specification developer2June 8, 2018000api.fda.gov
Schoelly Fiberoptic, GMBHDENZLINGEN Baden-Wurttemberg, GermanyManufacturer2October 8, 2020010api.fda.gov
RZ Medizintechnik GMBHTUTTLINGEN Baden-Wurttemberg, GermanyContract manufacturer, Specification developer1June 3, 2025000api.fda.gov
asap endoscopic products GmbHUmkirch Baden-Wurttemberg, GermanyContract manufacturer, Manufacturer1September 29, 2003000api.fda.gov
Boyd Weiler GmbH & Co. KGWeiler-Simmerberg Bavaria, GermanyContract manufacturer0000api.fda.gov
Erbe Vision GmbHSEXAU Baden-Wurttemberg, GermanyContract manufacturer0000api.fda.gov
Eurofins STERIPAC GMBHCalw-Altburg Baden-Wurttemberg, GermanyContract manufacturer0000api.fda.gov
Jr-Medizintechnik GMBH & Co KGLeibertingen Baden-Wurttemberg, GermanyContract manufacturer0000api.fda.gov
Karl Storz Se & Co. KGTUTTLINGEN 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
Koscher & Wuertz GMBHSPAICHINGEN Baden-Wurttemberg, GermanyContract manufacturer0000api.fda.gov
Olympus Winter & Ibe GmbHTELTOW Brandenburg, GermanySpecification developer0000api.fda.gov
Pajunk GMBH MedizintechnologieGEISINGEN Baden-Wurttemberg, GermanyContract manufacturer0000api.fda.gov
Strub Medical GmbH & Co. KGNEUHAUSEN Baden-Wurttemberg, GermanyContract manufacturer0000api.fda.gov
Tontarra Medizintechnik GMBHWURMLINGEN Baden-Wurttemberg, GermanyContract manufacturer0000api.fda.gov
Vomed Volzer Medizintechnik GMBH & Co.kgTuttlingen 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.