Latest Announcement

Compremium Corp. Receives FDA clearance for the CPMX1 System

Switzerland based Compremium Corp. announces U.S. Food and Drug Administration FDA510k market clearance of its Compartmental Compressibility Monitoring System CPMX1.
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Compremium Corp. Receives FDA clearance for the CPMX1 System
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Turning Point in Diagnostics

1 out of 2 people in the world have a diagnostic condition related to pressure — our breakthrough innovation is here to help.
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CHALLENGE

Until now, our only options have been subjective, unspecific, or invasive

Palpation
A subjective and unreliable clinical assessment.
Imaging
Imaging techniques are unspecific and not actionable.
Invasive Devices
Poor patient experience and risk of infection.
Solution

A non-invasive platform technology for the diagnosis of pressure-related conditions

Learn about the solution
Our methodology

Founded on game-changing methods for objective, actionable data points

Compressibility

Measure of relative change in the depth of a compartment when external pressure is applied

Occlusion Pressure

Method of assessing pressure at the point of occlusion for any vessel of interest
Learn about the science

Scientific validation

40
+
Publications
100
+
Authors
400
+
Study participants
10
+
Anatomical structures
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ISO 13485 Certification: A commitment to quality and innovation

We are pleased to announce that we have successfully obtained the ISO 13485:2016 certification for our quality management system (QMS). This significant milestone reflects our commitment to maintaining the highest standards in the design and development of medical devices for our novel, non-invasive measurement solutions.

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CPMX1 is MIL-STD 810H compliant and ready for duty

Compremium has achieved the next milestone: CPMX1 has successfully passed rigorous testing and is now capable of measuring and monitoring pressure-related conditions in austere environments.

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Important advancement in pediatric diagnostics

by compremium team

Clinical study with Compremium's non-invasive method on 25 pediatric patients suggests an easy and secure approach that has the potential to eliminate the need for invasive measurement of suspected Acute Compartment Syndrome (ACS).

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