Jaw Motion Import

Jaw Motion Import

ChairsideCAD Add-on Module

Upcoming with ChairsideCAD 2.3 Matera

Import jaw measurement from devices

The Jaw Motion Import  module allows you to import jaw movement registration data from external devices such as the JMA system from Zebris. 

The add-on module works in combination with the Auto Articulator Module. For experts: combine with Model Creator  to create innovative, semi-dynamic physical models.

Transfer your patient‘s actual, dynamic jaw movements into the software. Simulate them during the design process and create custom-fit restorations.

Example of Jaw Motion hardware
Combination with the Model Creator module
Transfer of the patient’s actual, dynamic jaw movements into the software. Play them back and create restorations that consider the true movements.
Jaw movement visualized in software


Read more about the core version or get in touch with our sales partners for pricing details.

ChairsideCAD  core version  and  Find your reseller


ChairsideCAD Add-on Modules

Medical Device Software exclusively available with Flex License

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.