Adler Ortho S.p.A

Adler Ortho S.p.A specializes in orthopedic implants for joint reconstruction. Their portfolio includes modular femoral and tibial components like the CO-CR HEADS and APTA STEM, spinal fixation devices such as FOOT SCREWS, and customizable systems for knee and hip replacements, including the DREAM and OMNIA. They also produce modular acetabular components (e.g., PANTHEON PHR) and mobility-enhancing devices like the BIS MOBILITY system, all designed for hip arthroplasty.

Adler Ortho S.p.A is headquartered in Italy, where it develops and manufactures its orthopedic implant products. The company’s location aligns with EU regulatory frameworks, ensuring compliance with local and regional medical device standards.

Adler Ortho S.p.A’s devices are registered in the eudamed database, the official EU portal for medical device information under the Medical Device Regulation (MDR). This registry ensures transparency and traceability of high-risk orthopedic implants, including those classified as Class IIb and Class III.

Adler Ortho S.p.A’s devices are classified as Class IIb and Class III under EU medical device regulations. This classification reflects their higher-risk nature, particularly for orthopedic implants used in joint reconstruction and spinal fixation, requiring stricter compliance with safety, performance, and clinical evaluation requirements.