Philips Zenition 30 Mobile C-arm Receives FDA Approval, Enhancing Surgical Procedures

Koninklijke Philips (PHG) has received FDA 510(k) approval for its Zenition 30 mobile C-arm, a device that enables image-guided surgical procedures with greater control and image clarity. The device addresses staff shortages and financial constraints in hospitals, improving patient access and reducing waiting periods. The Zenition 30 is designed to provide surgeons with more customization and flexibility, allowing them to focus on patient care amidst a global image guided surgery devices market that is projected to reach $17.2 billion by 2032.

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