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Data / Medical devices / Dispenser, Liquid Medication / Germany

FDA-registered makers of Dispenser, Liquid Medication in Germany: 6 establishments

6 establishments in Germany are registered with the FDA to make Dispenser, Liquid Medication (product code KYX). 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
Dispenser, Liquid Medication
Product code
KYX
Country
Germany

Makers of Dispenser, Liquid Medication in Germany

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Almo-Erzeugnisse Erwin Busch GMBHBAD AROLSEN Hesse, GermanyContract manufacturer0000api.fda.gov
B. Braun Melsungen AGMELSUNGEN Hesse, GermanyExporter to the US, Specification developer0000api.fda.gov
Elm-Plastic GMBHDudeldorf Rhineland-Palatinate, GermanyContract manufacturer, Manufacturer0000api.fda.gov
Henke-Sass Wolf, GMBH.TUTTLINGEN Baden-Wurttemberg, GermanyContract manufacturer, Manufacturer0000api.fda.gov
Joimax GMBHKARLSRUHE Baden-Wurttemberg, GermanyExporter to the US, Manufacturer0000api.fda.gov
Silgan Dispensing Systems Hemer GmbHHEMER North Rhine-Westphalia, GermanyManufacturer0000api.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.