Scan
Seconds
Contactless 3D scanning replaces plaster casting. A faulty scan is spotted instantly and repeated; the patient is measured in a single session.
How It Works
Clonify is not a fully autonomous black box: it is clinician-approved guided automation. Here you can transparently see the four steps from scan to production — and who decides at each step.
Seconds
Contactless 3D scanning replaces plaster casting. A faulty scan is spotted instantly and repeated; the patient is measured in a single session.
Automatic
Anatomical alignment is automatic; in cranial cases CVAI, cephalic index, volume and circumference are computed on their own.
Minutes
The system suggests the design step by step; clinical decisions such as trimlines and regional shaping always pass through clinician approval.
One click
The approved design goes as a millimetrically sliced file to the clinic's printer or a partner manufacturing center.
Transparency
In medical software, trust starts with not hiding what is automated. Every row in this table is how the product works today.
Anatomical alignment (cranial)
Computed automatically; the clinician reviews, approves and can correct.
Asymmetry & anthropometry (CVAI, cephalic index, volume, circumference)
Fully automatic measurement + threshold-based severity classification; reports auto-generated.
Pre/post treatment comparison report
Two scans are compared automatically; a PDF/Excel clinical report is produced.
AFO mold preparation and foot plane alignment
Automatic suggestion; trim and final shaping require the clinician's decision.
Anatomical landmarks and trimlines
The system offers a starting suggestion; the final line is a clinical decision the user approves.
Shell thickness, ventilation, production file
Automatic with default parameters; the clinician can make regional changes.
Regional shaping (relief/pressure zones)
Requires clinical judgement; the software provides precise tools, not the decision.
Diagnosis and treatment decision
A deliberate design choice: the system suggests classifications, it does not diagnose.
Transition
Week 1
Hardware setup and team training (target: ≤8 hours). First scans are done as shadow work.
Weeks 2–3
The plaster flow is not shut down; selected cases run through both methods in parallel and results are measured together.
Week 4
The team designs unassisted; remote co-design support continues for the first 10 devices.
Your approved design file is sent to an ISO 13485-certified partner manufacturing center; the device ships to your clinic. Start the digital flow today without hardware investment and move to your own printer as volume grows.
Bring a scan of your own patient to the demo; let's walk the four steps together.
Your data is hosted in Türkiye
A clinician approves every step
Compliant with custom-made device regulation