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Data / Medical devices / Syringe, Piston / Germany

FDA-registered makers of Syringe, Piston in Germany: 7 establishments

7 establishments in Germany are registered with the FDA to make Syringe, Piston (product code FMF). 4 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
Syringe, Piston
Product code
FMF
Country
Germany

Makers of Syringe, Piston in Germany

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
B. Braun Melsungen AGMELSUNGEN Hesse, GermanyExporter to the US, Manufacturer, Specification developer6March 5, 2020000api.fda.gov
Arthrex GmbHMunich Bavaria, GermanyExporter to the US, Specification developer3May 16, 2012000api.fda.gov
Haselmeier GMBHSTUTTGART Baden-Wurttemberg, GermanySpecification developer1March 21, 2007000api.fda.gov
Henke-Sass Wolf, GMBH.TUTTLINGEN Baden-Wurttemberg, GermanySpecification developer1May 28, 1982000api.fda.gov
Almo-Erzeugnisse Erwin Busch GMBHBAD AROLSEN Hesse, GermanyContract manufacturer0000api.fda.gov
Friedrich Daniels GMBHSOLINGEN North Rhine-Westphalia, GermanyContract manufacturer0000api.fda.gov
Transcoject GMBHNEUMUENSTER Schleswig-Holstein, 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.