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Last updated: Nov 20, 2024
Last updated: Dec 16th, 2025
On the 20th of November, 2024 we are updating our Terms of Sale and Terms of Use. These amendments will help you better understand how our DM Software Products and Services work.
You can find the updated Terms of Use and Terms of Sale at the bottom of this page.
In summary, please find below the main changes
We have updated the list of our products and services to reflect the deletion of the ones we stopped providing and add the new ones launched or modified in 2024. We added some wording relating to the implementation of multifactor authentication to further strengthen cybersecurity. We have reinforced the conditions of use of our products, notably due to their status as medical devices.
Please feel free to contact our Legal Team at legal@dental-monitoring.com should you need further information
On the 16th of December, 2025 we are updating our Terms of Sale, Terms of Use and Privacy Policy. These amendments will help you better understand how our DM Software Products and Services work.
You can find the updated Terms of Use, Terms of Sale and Privacy Policy at the bottom of this page.
In summary, please find below the main changes :
The list of our DM Products and Services has been updated to remove discontinued items and to include newly launched or modified offerings for 2025. We have also expanded certain provisions to clarify the warranties applicable and the importation requirements for DM Hardware Products based on country-specific regulations, and the extent of DM’s responsibility for all our DM Products and Services.
The list of our DM Products and Services has been updated to remove discontinued items and to include newly launched or modified offerings for 2025. We have updated the eligibility requirements for accessing and using our DM Software Products and Services. We have also added information regarding our AI systems to align with the new AI Act, which is progressively entering into force in Europe. In addition, we have clarified the conditions and requirements for using our Hardware Products, as well as the extent of DM’s responsibilities in the context of API integrations with PMS service providers.
We have updated our Privacy Policy to clarify and further explain our existing data processing activities. We have also included additional information about our AI systems to align with the new AI Act, which is progressively entering into force in Europe. Finally, we have added specific provisions applicable to public organisations using our DM Products and Services.
On the 16th of December 2025, you will be prompted to read and accept these three updated documents in the DM Platform or DM App. Accepting these are mandatory to continue using the DM Software Products and Services.
Please feel free to contact our Legal Team at legal@dental-monitoring.com should you need further information.
DentalMonitoring is a product designed and manufactured by Dental Monitoring SAS, for Healthcare Professionals (HCPs). It is also used by patients under the mandatory supervision of Healthcare Professionals (HCPs).
DentalMonitoring is designed to assist HCPs with remotely observing intraoral situations and monitoring orthodontic treatments. Refer to your HCP and/or the Instructions for Use before use. Some modules of the DentalMonitoring product are considered as a medical device (in Europe and other countries), registered as such and holding the CE mark. Product availability, claims and regulatory status may differ across countries depending on local regulations. Contact your local representative for further information.
DentalMonitoring is a product designed and manufactured by Dental Monitoring SAS, for Healthcare Professionals (HCPs). It is also used by patients under the mandatory supervision of Healthcare Professionals (HCPs).
DentalMonitoring is designed to assist HCPs with remotely observing intraoral situations and monitoring orthodontic treatments. Refer to your HCP and/or the Instructions for Use before use. Some modules of the DentalMonitoring product are considered as a medical device (in Europe and other countries), registered as such and holding the CE mark. Product availability, claims and regulatory status may differ across countries depending on local regulations. Contact your local representative for further information.