FDA 510(k) Applications Submitted by AnX Robotica Corp.

FDA 510(k) Number Submission Date Device Name Applicant
K230694 03/13/2023 NaviCam Xpress Stomach System, NaviCam Xpress System AnX Robotica Corp.
K191087 04/24/2019 IntraMarX Radiopaque Markers AnX Robotica Corp.
K201106 04/24/2020 IntraMarX 3D Radiopaque Marker AnX Robotica Corp.


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