Proprio Secures Second FDA Clearance for AI Surgery Platform

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Proprio has received a second FDA 510(k) clearance for its Paradigm surgical guidance platform, now enabling real-time intraoperative measurements for the first time in surgical history.

Key Advancements:

  • Dynamic 3D visualization and continuous intraoperative data
  • Real-time tracking of progress against pre-op plans
  • Empowers surgeons to measure success during surgery
  • Reduces revision surgeries and improves outcomes

Unlike traditional navigation tech, Paradigm allows uninterrupted focus on the patient by delivering data-driven decision support and multimodal views of anatomy. It marks a shift from estimation to precise, AI-assisted surgical planning and execution.

“This is game-changing,” said Gabriel Jones, CEO of Proprio. “We’re not just automating — we’re calibrating cognition, optimizing OR workflows, and reducing risks across the board.”

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