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Anx Robotica Corp

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
7
Inspections
2
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K241934NaviCam Xpress Stomach Capsule Endoscope System (NaviCam Xpress Stomach System) with NaviCam StomachJuly 31, 2024
K230694NaviCam Xpress Stomach System, NaviCam Xpress SystemApril 13, 2023
K221608NaviCam Capsule Endoscope System with NaviCam Stomach Capsule and NaviCam Tether, NaviCam Xpress StoNovember 22, 2022
K203192NaviCam Xpress Stomach SystemMay 4, 2021
DEN190037NaviCam Capsule Endoscope System with NaviCam Stomach CapsuleMay 22, 2020
K201106IntraMarX 3D Radiopaque MarkerMay 21, 2020
K191087IntraMarX Radiopaque MarkersDecember 18, 2019