FDA Clears V-PRO maX 2: A Breakthrough in Sterilizing 3D Printed Healthcare Devices

Exciting news in healthcare innovation! The FDA has granted clearance to the groundbreaking V-PRO maX 2 Low Temperature Sterilization System. This cutting-edge system is a game-changer, as it's the first FDA-cleared solution with a specialty cycle designed specifically to sterilize 3D printed devices in healthcare facilities.

Gone are the challenges of ensuring the safety of complex 3D printed surgical instruments and anatomical models. The V-PRO maX 2 system's specialty cycle is tailored to effectively sterilize patient-specific surgical guides, including those for osteotomy, shoulder, hip, knee, and spine procedures. These instruments, as well as anatomical models, are fabricated using 3D printing processes and are intended for single-use during surgical procedures.

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