The non-invasive ultrasound-based medical device

DXT by RESPINOR

  • Novel, non-invasive ultrasound device for accurate and continuous diaphragm monitoring
  • Enables early detection of diaphragm dysfunction in critical care settings
  • Successfully validated in clinical studies on mechanically ventilated patients
  • Backed by substantial funding from H2020 and The Research Council of Norway
  • CE-marked and EN ISO 13485:2016 certified, ensuring regulatory compliance and quality
  • Ready for global market adoption with ongoing efforts towards US authorization
  • Targets a market potential of over 350 million patients across US and EU
  • Developed to become the technology of choice for assessing work of breathing
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What is DXT?

DXT, or Diaphragm Excursion Technology, is a groundbreaking non-invasive medical device developed by RESPINOR that utilizes ultrasound for operator-independent, continuous monitoring of the diaphragm, the main breathing muscle, in critically ill patients.

This technology aids in the early detection of diaphragm dysfunction and enhances clinical decision-making in critical care settings.

The DXT Monitor

Key Benefits and Clinical Applications of DXT

Recent updates from RESPINOR

February 12, 2026

RESPINOR Signs Distributor Agreement with Eden Medical for RESPINOR DXT®, for England, Scotland and Wales

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December 1, 2025

RESPINOR Signs Distributor Agreement with Arseus Medical for RESPINOR DXT, for Belgium, the Netherlands, and Luxembourg.

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August 4, 2025

RESPINOR Secures CE Mark for RESPINOR DXT Under EU MDR – Enabling European Market Launch

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November 22, 2024

The FDA has designated RESPINOR DXT as a Breakthrough Device

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July 16, 2024

Operator independent continuous ultrasound monitoring of diaphragm excursion predicts successful weaning from mechanical ventilation: a prospective observational study, Demoule et al. Critical Care (2024) 28:245.

RESPINOR has successfully completed the clinical evidence program for the first indication, weaning from mechanical ventilation (MV), and is now preparing for regulatory submission both in Europe and the US.
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