July 25, 2018

Adaptiiv Medical Technologies is delighted to announce the promotion of Adam Dennis to Director of Technology. Adam is a widely respected team leader and has made significant contributions to the growth of Adaptiiv since joining in Sept 2017. Adam has played an integral role in obtaining Adaptiiv’s recent FDA 510 (k) clearance.

Adam has a stellar reputation as a leader who is highly skilled, collaborative, innovative and set to help steer Adaptiiv in developing new technologies that will continue to improve treatment outcomes and patient experience.

Congratulations, Adam!



Adaptiiv Medical Technologies Inc. has received 510(k) clearance from the U.S. Food and Drug Administration (FDA) to market 3D Bolus Software. The company also has a CE Mark, ISO 13485 and TGA (Australia) approvals for its advanced software solution that enables the creation of customized personal medical devices using 3D printing.