Anx Robotica Corporation - FDA 510(k) Cleared Devices
Recent clearances: MotiliCap GI Monitoring System, NaviCam Small Bowel Capsule Endoscopy System with NaviCam SB Capsule and NaviCam Tether, NaviCam Xpress Stomach Capsule Endoscope System (NaviCam Xpress Stomach System) with NaviCam Capsule and NaviCam Tether
3
Total
3
Cleared
0
Denied
FDA 510(k) Regulatory Record - Anx Robotica Corporation Gastroenterology & Urology ✕
3 devices
Cleared
May 21, 2025
MotiliCap GI Monitoring System
Gastroenterology & Urology
90d
Cleared
Jan 05, 2024
NaviCam Small Bowel Capsule Endoscopy System with NaviCam SB Capsule and...
Gastroenterology & Urology
99d
Cleared
Oct 03, 2023
NaviCam Xpress Stomach Capsule Endoscope System (NaviCam Xpress Stomach...
Gastroenterology & Urology
92d