FDA Clearance of Arcam's EBM Technology

U.S. implant manufacturers have recently received FDA’s clearance for products manufactured with Arcam’s EBM® technology. With the FDA clearance the companies are allowed to market their products on the important U.S. market.

The U.S. market for orthopaedic implants represents about half of the world-wide implant market. Up to now U.S. sales of orthopaedic products manufactured with Arcam’s EBM ® technology have been limited to patient-specific implants, which do not require clearance. Arcam already has systems installed for orthopaedic applications at four U.S. companies. These recent FDA clearances open up a market with a large potential, and are a further confirmation that implants produced with the Arcam technology fulfil the high standards and demands in the orthopaedic implant industry.

PLUS, a new case study highlights of integrated tabecular structure for Fix Ti-Por acetabular cup.

New orthopaedic implants improve people’s quality of life
The CE-certified Fixa Ti-Por acetabular cup...Manufactured with an integrated trabecular structure for improved osseointegration.

Read the case study HERE.