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Data / Medical devices / System, Measurement, Blood-Pressure, Non-Invasive / Netherlands

FDA-registered makers of System, Measurement, Blood-Pressure, Non-Invasive in the Netherlands: 6 establishments

6 establishments in the Netherlands are registered with the FDA to make System, Measurement, Blood-Pressure, Non-Invasive (product code DXN). 4 have a 510(k) clearance or PMA approval on file and 1 has a recall event. FDA data exported November 2, 2026.

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Device
System, Measurement, Blood-Pressure, Non-Invasive
Product code
DXN
Country
Netherlands

Makers of System, Measurement, Blood-Pressure, Non-Invasive in the Netherlands

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Edwards Lifesciences Holding B.V.AMSTERDAM Noord-Holland, NetherlandsSpecification developer3June 13, 2014000api.fda.gov
Masena Invest, BVDordrecht Zuid-Holland, NetherlandsSpecification developer3June 19, 2013000api.fda.gov
Finapres Medical Systems B.V.Enschede Overijssel, NetherlandsManufacturer1November 6, 2018010api.fda.gov
Lode B.V.Groningen, NetherlandsManufacturer1June 7, 2006000api.fda.gov
Corsano Health B.V.The Hague Zuid-Holland, NetherlandsManufacturer0000api.fda.gov
Demcon Production B.V.Enschede Overijssel, NetherlandsContract 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.