Planning ACL reconstruction with confidence

Comprehensive 3D planning insights for revision ACL reconstruction and other joint preservation procedures.

INSIGHTFUL PLANNING

Our innovative system based on years of research, allows for precise and reproducible 3D assessment of ACL tunnel position, size and orientation.

ENHANCED VISIBILITY

Designed to give you enhanced visibility and guidance on optimal tunnel placement, our protocol and our proprietary modelling calculations give clinicians confidence and data-based insights.

INTERNATIONALLY PEER REVIEWED

Our internationally peer-reviewed protocol allows for an objective assessment of knee anatomy and pathology that facilitates optimal ACL tunnel placement for clinicians.

UNPARALLED PRECISION

Provides an objective assessment of knee anatomy & pathology that facilitates optimal ACL tunnel placement, providing clinicians with a new standard in efficiency and quality for ACL revision procedures.
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How it works

A new approach with complete visibility. Advanced modelling and clear visualisation facilitating optimal tunnel placement.

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Planning

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3d Models

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Allograft

Our advanced 3D planning begins with precise imaging and engineer analysis to map each patient’s unique anatomy, including ACL tunnel orientation and dimensions. This supports an objective, structured approach for ACL revision planning.

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Our advanced 3D planning begins with precise imaging and engineer analysis to map each patient’s unique anatomy, including ACL tunnel orientation and dimensions. This supports an objective, structured approach for ACL revision planning.
Dedicated to Delivering Personalised Precision, from Sydney to the world with our globally approved workflows

Our Story

Founded through a collaboration between surgeons, engineers, and industry experts. Built in Australia and growing globally, we believe in precision powered by people.

Our Team

Our engineers bring deep, clinical understanding and technical expertise to every procedure.

Comprehensive global quality and regulatory clearance

Regulatory clearance for patient-specific biomodels, guides and implants for any anatomical region

  • ISO 13485:2016

  • FDA 510k

  • Medical Device Single Audit Program

Start your personalised journey today, talk to our team about your next case.

Start your personalised journey today, talk to our team about your next case.

Start your personalised journey today, talk to our team about your next case.