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Stemell®’s Allografts and Autografts products (homologue use only) are manufactured terminally and diligently under sterilized and fully protected environment to enhance safety related to microbiological, viral transmission or any other contaminations. We manufacture our products in a fully certified Class 100 cleanroom. Our trained technicians operate under Good Laboratory Practices, Good Tissue Practices and Good Manufactured Practices regulations and requirements in order to make sure the company maintains all high standards to move toward our vision and quality promises. Stemell® uses fully medical graded materials to package its products which is highest standard in allografts products. All StemL™ materials are made in class 1000 clean room. In light of the media attention and in the wake of concerns related to the Chagas Disease Stemell® reiterates its long-standing processing safety standards for the terminal sterilization of Stemell® allografts products. The Stemell® flagship allografts have always been terminally sterilized, and the Company’s proprietary StemL™ products processes have continually used terminal sterilization as an essential part of the process.