With more than 20 years of experience in tissue engineering, TETEC develops personalized cell therapies for the treatment of knee cartilage defects, with the aim of preserving joint function and supporting patients’ long-term mobility, independence, and quality of life. Learn more by selecting the information most relevant to you.
As part of the Octane Medical Group, we are continuously advancing established procedures for biological cartilage repair while developing innovative technologies that could make autologous cell transplants more efficient and bring these advanced therapies closer to the point of care in the future. Our goal is to further improve treatment options for patients with cartilage defects and support the future use of regenerative cell therapies in additional medical indications.
TETEC offers two matrix-associated autologous chondrocyte transplantation (MACT) procedures for the treatment of knee cartilage defects: Injectable MACT and Scaffold-Based MACT.

Injectable MACT is a cell-based procedure for the treatment of focal cartilage defects of the knee. The procedure uses a patient's own cartilage cells in combination with an injectable hydrogel for transplantation into the cartilage defect [1]. In clinical studies and earlier publications, this procedure has also been referred to as hydrogel-based ACI or Injectable M-ACI.

In Scaffold-Based MACT, a patient's own cartilage cells are seeded onto a collagen-based scaffold and transplanted into the cartilage defect [2].
Autologous cell transplants manufactured by TETEC have been used in more than 30,000 autologous chondrocyte transplantation procedures in Germany for the treatment of focal cartilage defects of the knee [3].
TETEC partners with leading academic, clinical, and industrial organizations to advance research and therapeutic development in regenerative medicine.
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Join our team and help shape the future of regenerative medicine. We offer a wide range of opportunities in manufacturing, quality assurance, and research, all focused on advancing personalized cell therapies for the treatment of cartilage defects of the knee.
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1. TETEC AG. Summary of Product Characteristics (SmPC) NOVOCART® Inject. Reutlingen (DE): TETEC AG; 2026. Revision date: 02/2026. PEI.A.11763.01.1.
2. TETEC AG. Summary of Product Characteristics (SmPC) NOVOCART® 3D. Reutlingen (DE): TETEC AG; 2023. Revision date: 11/2023. PEI.A.11511.01.1.
3. TETEC AG. Internal registry and documentation of Injectable MACT and Scaffold-Based MACT procedures performed in Germany. Reutlingen (DE): TETEC AG; 2025.