Data / Medical devices / System, Measurement, Blood-Pressure, Non-Invasive / Germany
FDA-registered makers of System, Measurement, Blood-Pressure, Non-Invasive in Germany: 11 establishments
11 establishments in Germany 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 0 have a recall event. FDA data exported November 2, 2026.
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- Device
- System, Measurement, Blood-Pressure, Non-Invasive
- Product code
- DXN
- Country
- Germany
Makers of System, Measurement, Blood-Pressure, Non-Invasive in Germany
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Rudolf Riester GMBH | JUNGINGEN Baden-Wurttemberg, Germany | Manufacturer, Repackager or relabeler | 7 | June 24, 2019 | 0 | 0 | 0 | api.fda.gov |
| Iem GMBH | Aachen North Rhine-Westphalia, Germany | Contract manufacturer, Manufacturer | 3 | May 16, 2019 | 0 | 0 | 0 | api.fda.gov |
| PAR MEDIZINTECHNIK GMBH & Co. KG | Berlin, Germany | Manufacturer | 2 | June 14, 2017 | 0 | 0 | 0 | api.fda.gov |
| Seca | Hamburg, Germany | Manufacturer | 1 | January 23, 2020 | 0 | 0 | 0 | api.fda.gov |
| GWW | Gaertringen Baden-Wurttemberg, Germany | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Heine Optotechnik GMBH & Co. KG. | GILCHING Bavaria, Germany | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Nicolay GMBH | NAGOLD Baden-Wurttemberg, Germany | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Pulsion Medical Systems Se | Aschheim, Germany | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Philips Medizin Systeme Boeblingen GmbH | BOEBLINGEN Baden-Wurttemberg, Germany | Complaint file establishment, Manufacturer, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Somnomedics AG | RANDERSACKER Bavaria, Germany | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Siemens Healthineers AG | FORCHHEIM Bavaria, Germany | Exporter to the US, Manufacturer | 0 | 0 | 0 | 0 | api.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.