Even designing abutment and suprastructures in one single CAD session is possible. Angulated screw channels are supported as well.
With Implant Module, the choice is yours! Either mill in-house or send out your files for production. The add-on module supports a wide range of in-house milling systems. In addition, leading production centers will accept files generated by exocad software.
Flexible design options for various types of implant-based restorations.
The proven exocad wizard guides you through the different steps of the design process.
exocad’s Implant Module is delivered with an extensive set of implant libraries and supports a huge selection of implant systems – from top-tier implant manufacturers to smaller local players. There is an even wider range of titanium bases from third-party manufacturers to choose from. In addition, many milling centers provide dedicated libraries for exocad’s Implant Module.
exocad.com/library-integration
Read more about the core version or get in touch with our sales partners for pricing details.
ChairsideCAD core version and Find your reseller
We offer all Medical Device Software (including ChairsideCAD and exoplan) exclusively via a subscription-based licensing model. The reason is that our Medical Device Software should always be under maintenance, so that in the unlikely event of a safety issue with the product, an update of the software can be provided. Our policy has always been to provide maintenance free of charge for one year after the initial purchase of our software, and to provide software updates only for licenses that are currently under maintenance. While we do provide permanent licenses for our non-medical products (such as exocad DentalCAD, targeted at dental labs), which users can continue to use indefinitely even out of maintenance, this is not the case for our Medical Device Software. These products will no longer function if subscription is not renewed. Permanent licenses – which can be used indefinitely – are not available for our Medical Device Software. According to MDD 93/42/EEC, Annex I, Requirement 4, which applies to these products, all medical devices must have a determined lifetime.
