Adaptiiv Medical Technologies Inc.

Adaptiiv software allows practitioners to provide personalized care via the creation of patient-specific 3D printed devices used in radiation therapy. 3D printed devices improve clinical precision as they conform to complex anatomy to improve dose delivery while sparing healthy tissues. Achieve operational efficiency gains as 3D printed devices are produced quickly and the integration of Adaptiiv's solution with clinical workflows reduce patient consult and set up times. Adaptiiv has received 510(k) regulatory clearance from the U.S. Food and Drug Administration (FDA) to market its software for use in radiation oncology. The company also has a CE Mark and ISO 13485 certification