Privacy Policy &
Our Methodology

When you interact with Akrolimb, we may collect the following categories of information:

• Contact details — name, email address, phone number, and clinic or organisation name when you submit enquiries, request demos, or register for an account.
• Usage data — anonymised analytics on how you navigate our website, including pages viewed and session duration, to improve our services.
• Clinical workflow data — scan data, design parameters, and device specifications processed through our software platform, used solely for device production and quality assurance.

• To provide, maintain, and improve our design software and manufacturing services.
• To respond to enquiries, process demo requests, and provide customer support.
• To ensure device quality and traceability as required by applicable medical device regulations.
• To conduct anonymised analysis for improving our design algorithms and manufacturing processes.

We do not sell, rent, or share your personal data with third parties for marketing purposes. Data processed through our clinical workflow is treated as confidential and handled in accordance with relevant data protection laws.

We implement appropriate technical and organisational measures to protect your information, including:

• Encrypted data transmission and storage for all clinical and personal data.
• Role-based access controls limiting data visibility to authorised personnel only.
• Regular review of our data handling practices in line with our quality management procedures.

Under applicable data protection legislation, you have the right to:

• Access the personal data we hold about you.
• Request correction of inaccurate or incomplete data.
• Request deletion of your data, subject to any legal retention requirements.
• Withdraw consent for marketing communications at any time.

To exercise any of these rights, contact us at info@akrolimb.com.

Our workflow begins with a precise 3D scan of the patient's anatomy. This data is processed through our proprietary design software, which assists clinicians in generating a custom device model tailored to the individual's biomechanical needs.

The software incorporates clinical parameters and design rules developed through iterative testing with practising clinicians and rehabilitation professionals. This digital-first approach eliminates the need for traditional plaster casting, significantly reducing turnaround time and material waste.

Before manufacturing, each device design undergoes computational analysis to verify structural integrity under expected loading conditions. This simulation step identifies potential weak points and ensures the design meets our durability and safety thresholds.

Our pre-production validation protocol was developed through extensive testing and refined during clinical deployments where devices were fitted and evaluated by real users in everyday conditions. The combination of computational checks and field-validated design rules gives us confidence in the performance of every device before it is printed.

Devices are produced using additive manufacturing (3D printing) with process parameters that have been carefully calibrated to achieve the right balance of strength, flexibility, weight, and surface finish for clinical use.

Our manufacturing profiles are the result of systematic material and parameter optimisation, ensuring consistent quality across production runs. This controlled process is what enables us to deliver clinical-grade devices at a fraction of traditional manufacturing costs, with significantly faster turnaround times.

All cost savings and performance claims presented on this website are informed by real-world deployments across clinical and humanitarian settings. We have fitted devices to users through partner clinics and organisations, collecting feedback on comfort, functionality, and durability.

These deployments serve as the foundation for our pricing models and production estimates. We continuously refine our process based on user outcomes and clinician feedback.