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Data / Medical devices / Device, Monitoring, Intracranial Pressure / Germany

FDA-registered makers of Device, Monitoring, Intracranial Pressure in Germany: 7 establishments

7 establishments in Germany are registered with the FDA to make Device, Monitoring, Intracranial Pressure (product code GWM). 2 have a 510(k) clearance or PMA approval on file and 1 has a recall event. FDA data exported November 3, 2026.

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Device
Device, Monitoring, Intracranial Pressure
Product code
GWM
Country
Germany

Makers of Device, Monitoring, Intracranial Pressure in Germany

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
RAUMEDIC - MuenchbergHelmbrechts Bavaria, GermanyManufacturer, Specification developer6August 29, 2025000api.fda.gov
SPIEGELBERG GmbH & Co. KGHamburg, GermanyManufacturer1June 28, 2001010api.fda.gov
Gebr. Brasseler GMBH & Co. KGLEMGO North Rhine-Westphalia, GermanyContract manufacturer0000api.fda.gov
Hipp Medical AGRenquishausen Baden-Wurttemberg, GermanyContract manufacturer0000api.fda.gov
RAUMEDIC - Werk ZwoenitzZwoenitz Saxony, GermanyContract manufacturer0000api.fda.gov
Reco Medizintechnik Wolfgang Rentsch EkPirna Saxony, GermanyContract manufacturer0000api.fda.gov
Rudolf Storz GMBHEMMINGEN Baden-Wurttemberg, GermanyContract manufacturer0000api.fda.gov

Updated November 3, 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.