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Data / Medical devices / Dispenser, Cement / Germany

FDA-registered makers of Dispenser, Cement in Germany: 8 establishments

8 establishments in Germany are registered with the FDA to make Dispenser, Cement (product code KIH). 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, Cement
Product code
KIH
Country
Germany

Makers of Dispenser, Cement in Germany

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Armbruster GMBHSteinach Baden-Wurttemberg, GermanyContract manufacturer0000api.fda.gov
Heraeus Medical GmbHWEHRHEIM Hesse, GermanyManufacturer0000api.fda.gov
Moeller Medical GMBHFULDA Hesse, GermanyManufacturer0000api.fda.gov
Osartis GMBHMuenster Hesse, GermanyManufacturer0000api.fda.gov
PROMOTEC-MEDIZINTECHNIK GmbHBlankenfelde / Mahlow Brandenburg, GermanyContract manufacturer0000api.fda.gov
Puracon GMBHRosenheim Bavaria, GermanyContract manufacturer0000api.fda.gov
Silony Medical GMBHLeinfelden-Echterdingen Baden-Wurttemberg, GermanyManufacturer, Specification developer0000api.fda.gov
Spang & Brands GMBHFriedrichsdorf Hesse, 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.