MensKey Complete
Gain insights on chronic infections, revealing bacterial load and antimicrobial resistance genes with the MensKey Complete.

MicroGenDX is a molecular diagnostics company specializing in direct microbial DNA analysis using molecular methods—Next-Generation Sequencing (NGS) and PCR—combined with advanced bioinformatics. This approach enables the detection and identification of more than 50.000 bacterial and fungal organisms directly from clinical samples, including cases where conventional culture-based methods provide limited or inconclusive results
MicroGenDX supports healthcare professionals across multiple medical fields, including urology, gynecology, orthopedics, ENT, wound care, and infectious diseases, with a focus on chronic, recurrent, or complex infections.
MicroGenDX originated in the United States and has been advancing molecular infection diagnostics for over a decade. The technology has been further developed and clinically applied worldwide. Today, MicroGenDX tests are available in Europe through accredited laboratory partners, operating in accordance with European quality and regulatory standards.
To date, the MicroGenDX test has been applied on more than 750,000 clinical samples worldwide. The diagnostic workflow combines sequencing, curated microbial reference databases, and advanced bioinformatics to generate clinically interpretable laboratory reports. MicroGenDX works closely with clinicians and laboratory partners to support informed diagnostic and therapeutic decision-making.
MicroGenDX is committed to the evidence-based integration of molecular diagnostics into clinical practice. The company supports ongoing clinical research and has contributed to peer-reviewed publications evaluating DNA-based pathogen detection in comparison with conventional microbiological methods.
In Europe, MicroGenDX collaborates with accredited diagnostic laboratories to ensure testing is performed in compliance with applicable quality and regulatory frameworks, including:
All analyses are performed under defined quality control and validation procedures.