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Data / Medical devices / File, Pulp Canal, Endodontic / Germany

FDA-registered makers of File, Pulp Canal, Endodontic in Germany: 8 establishments

8 establishments in Germany are registered with the FDA to make File, Pulp Canal, Endodontic (product code EKS). 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
File, Pulp Canal, Endodontic
Product code
EKS
Country
Germany

Makers of File, Pulp Canal, Endodontic in Germany

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
BUSCH & CO. GmbH & Co. KGENGELSKIRCHEN North Rhine-Westphalia, GermanyContract manufacturer, Manufacturer0000api.fda.gov
Coltene/Whaledent GMBH & Co. KGLANGENAU Baden-Wurttemberg, GermanyManufacturer0000api.fda.gov
Gebr. Brasseler GMBH & Co. KGLEMGO North Rhine-Westphalia, GermanyManufacturer, Specification developer0000api.fda.gov
Hager & Meisinger GMBHNEUSS North Rhine-Westphalia, GermanyManufacturer0000api.fda.gov
Hager & Werken GMBHDUISBURG,DE-NOTA Hamburg, GermanyManufacturer0000api.fda.gov
Symmetry Surgical GmbHTUTTLINGEN Baden-Wurttemberg, GermanyContract manufacturer0000api.fda.gov
VDW GMBHMUNICH Bavaria, GermanyManufacturer0000api.fda.gov
Voco GMBHCUXHAVEN Lower Saxony, 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.