Skip to the page

Data / Medical devices / Bandage, Cast / Germany

FDA-registered makers of Bandage, Cast in Germany: 6 establishments

6 establishments in Germany are registered with the FDA to make Bandage, Cast (product code ITG). 0 have a 510(k) clearance or PMA approval on file and 1 has a recall event. FDA data exported November 2, 2026.

SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.

Device
Bandage, Cast
Product code
ITG
Country
Germany

Makers of Bandage, Cast in Germany

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Freudenberg Performance Materials GmbH & Co. KGWeinheim Baden-Wurttemberg, GermanyContract manufacturer, Exporter to the US0000api.fda.gov
KOB GmbHWolfstein Rhineland-Palatinate, GermanyContract manufacturer0010api.fda.gov
Lohmann & Rauscher GMBH & Co. KGNEUWIED Rhineland-Palatinate, GermanyManufacturer, Specification developer0000api.fda.gov
Ottobock SE & Co. KGaA formerly known as Otto Bock Healthcare GmbHDUDERSTADT Lower Saxony, GermanyExporter to the US, Specification developer0000api.fda.gov
Solventum Germany GmbHKamen North Rhine-Westphalia, GermanyComplaint file establishment, Exporter to the US, Specification developer0000api.fda.gov
Twe Dierdorf GMBH And Co. KGDierdorf Rhineland-Palatinate, 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.