Kuvia3D® provides three-dimensional renderings of knee bones and their articular cartilage, allowing physicians and patients to better understand MR imaging study results.  The knowledge gained from a 3D image can help in orthopedic pre-surgical planning, when clinically appropriate, and help facilitate patient communication. The software was 510k cleared by FDA in 2015 as a Class II medical device. In 2022, FDA provided guidance that Kuvia3D is now considered a “software function” which is not intended for diagnostic image review.

Produced under the supervision of a radiologist, the automated 3D renderings generated by Kuvia3D¹ allow physicians and patients to better see imaging study results as familiar anatomy rather than 2D cross sections.

Incorporating Kuvia3D into clinical practice is easy. The protocol can be an add-on MRI series (~4 mins.) to your routine clinical knee study, or a minor modification to one of your existing sequences.