The manufacturer's patient information states: ‘The application is intended to be used for filling clearly delimited cartilage damage up to grade IV in joints such as the knee, hip, shoulder and ankle as well as in partial cartilage injuries, subchondral and osteochondral defects. The implant offers the patient's own cells the opportunity to migrate into the matrix for the associated tissue regeneration. At the same time it serves as protection against further cartilage degeneration. Use in other parts of the body, such as auricle or breast, is not permitted.’
Manufactured by Meidrix Biomedicals GmbH, Esslingen, Germany. UK Responsible Person: Actomed Ltd, The Old Barracks, Sandon Road, Grantham NG31 9AX. Listed on the MHRA register of medical devices. Registration is not approval. CE marked by the manufacturer; accepted on the Great Britain market under the current transitional arrangements for CE-marked devices. Current instructions for use remain authoritative.
Report a suspected product quality or safety issue to Actomed, the UK Responsible Person.
Product, technique and clinical-evidence information on this site is written for UK healthcare professionals. Patients should discuss whether ChondroFiller is suitable with a treating clinic.
Date of preparation: September 2026.