- In February 2024, Pro Med Instruments GmbH (Germany) received U.S. FDA 510(k) clearance for its Skull Clamp system. This development introduces an ergonomically designed clamp with adjustable pin pressure for enhanced patient safety and surgical precision. It improves surgeon comfort and minimizes head movement during neurosurgical procedures. The clearance boosts Pro Med's presence in the U.S. and encourages wider adoption of advanced cranial fixation systems in operating rooms
