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ProVision Surgical
Home
Story
Members
Invest
Support
  • FAQs
  • Updates & Events
  • Contact Us
  • News
More
  • Home
  • Story
  • Members
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    • FAQs
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Welcome to Provision FAQ

We’re redefining orthopedic surgery with PAIR, our Augmented Intelligent Reality system that projects 3D anatomy and surgical plans directly into the surgeon’s view. Designed for precision, efficiency, and adaptability, PAIR brings real-time visualization and guidance to the operating room. 

Frequently Asked Questions

Please reach us at abahour@provisionsurgical.com if you cannot find an answer to your question.

 We’re developing an augmented reality (AR) platform that brings preoperative imaging and surgical planning directly into the surgeon’s view during procedures. It enables enhanced visualization, precision, and real-time guidance — improving accuracy and confidence in every step. 


Orthopedics presents some of the most demanding alignment and precision challenges. Joint replacement surgeries require exact implant positioning to ensure long-term outcomes. By starting here, we’re delivering immediate clinical value where visualization and accuracy make a measurable difference. 


Our system aims to improve surgical precision, reduce cognitive load, shorten operative time, and support better patient outcomes. Early evaluations suggest faster adjustments and more consistent implant alignment compared to standard methods. 


Traditional navigation systems can be bulky, costly, and disruptive. Our solution offers comparable accuracy in a lightweight, cost-effective format designed to integrate easily into existing workflows. 


No major changes are needed. The system is designed to complement standard techniques and integrate seamlessly, minimizing the learning curve while enhancing intraoperative visualization. 


Yes. The same AR visualization used in surgery supports surgical training by projecting anatomy and procedural steps in 3D — helping learners build spatial awareness and clinical precision in realistic, hands-on environments. 


Not yet. The FDA has approved our test plan for accuracy, reliability, and safety, and we are in the process of completing verification and validation testing ahead of submitting our 510(k) application for regulatory clearance. 


It confirms our regulatory pathway is progressing as planned. Hospitals and surgeons can have confidence that the system is undergoing rigorous testing for accuracy, reliability, and safety prior to clinical deployment. 


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