No system change.
Just a change of supplier.
Why your workflow remains unchanged.
The digital workflow knows no manufacturer. It only knows exact reference geometries. If an implant-prosthetic component – an abutment, for example – meets these geometries with high precision, the workflow in the dental laboratory remains unchanged. That is the principle of OrangeCAD MED.
The digital workflow in implant prosthetics is based on defined reference geometries. They determine how components are positioned, designed and manufactured. What is decisive is therefore not which manufacturer a component comes from, but whether it corresponds to these reference geometries.
OrangeCAD MED therefore implements these reference geometries within narrowly defined manufacturing tolerances. This is made possible by geometries captured with high precision, which are reproduced by means of reverse engineering; and that batch after batch.
The result for the dental laboratory: you change the component – not the workflow.
What stays. What changes.
- What stays: scan body, CAD library, design process, holder and machine.
- What changes: the component – and thus your cost-effectiveness.
Manufactured in Baden-Württemberg from a titanium alloy, with narrow manufacturing tolerances and reproducible fit – developed for modern CAD/CAM workflows.
No system change. Just a change of supplier.
OrangeCAD MED Komponenten passen auf alle gängigen Implantatsysteme und in jeden bestehenden CAD/CAM-Workflow. Scanbody, Library, Halter, Maschine: alles bleibt unverändert. Sie tauschen nur die Komponente aus. Das war’s.
Our story
Discover how 25 years of experience gave rise to OrangeCAD MED.
Expertise
Practical knowledge, background information and current trends in implant prosthetics.
Careers
Become part of a team that is rethinking implant prosthetics.
Lifetime warranty
Every component. Without restriction.
In combination with all common implant systems.
Made in Germany
Manufactured in Baden-Württemberg. Titanium alloy.
Tight manufacturing tolerances.
QM system in accordance with DIN EN ISO 13485
Our products meet the general safety and performance requirements of the MDR.
