LEM Surgical wins FDA clearance for hard tissue surgical robot

LEM Surgical announced that it received FDA 510(k) clearance for its Dynamis robotic surgical system for hard tissue surgery.

Bern, Switzerland-based LEM Surgical has its U.S. offices and a surgical demonstration suite for its robot in Tampa, Florida. It designed Dynamis as an integrated, navigation-based robotic platform. It enhances accuracy and control during spine surgeries. Clearance provides U.S. spine surgeons with the next-generation technology that combines real-time imaging, dynamic guidance and adaptable instrumentation compatibility within a single, versatile platform.

Dynamis features three robotic arms, with two for surgical guidance and one for optical navigation. They consolidate into a single cart that fits partially beneath the surgical table. Unlike currently available systems, LEM Surgical says its system supports a wide range of surgical instruments through unique, adjustable end-effectors and intraoperative qualification. This enhances compatibility and hospital workflow efficiency.

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