I.Ceram obtained the CE marking for its first new generation implant: The unloaded sternal implant. This certificate allows the company to market this product in the European Union and in many countries all over the world. This certification validates the quality of the work done and confirms the implant's qualities for biocompatibility, osseointegration and radiolucency, making it a reference product for sternal reconstruction surgery. This sternum made in porous alumina brings a unique solution for the treatment of sternal diseases such as tumors, metastases or infections. I.Ceram will start commercializing this implant in France and in foreign countries due to contracts signed with well-known distribution partners. The real differentiation between I.CERAM's sternal implant and conventional orthopedic products should allow the signing of more new agreements with commercial partners. The marketing strategy being implemented by I.Ceram, relies on distribution partnerships with companies specialized in medical devices sales for thoracic surgery. These partners will be responsible for presenting the product and providing ongoing support to the medical teams. As such, before this CE marking obtention, a workshop was organized for forty French and European surgeons in January 2018 at Mons University (Belgium). Another one is planned for European surgeons in Basel (Switzerland) mid-November.