Anx Robotica Corporation - FDA 510(k) Cleared Devices
3
Total
3
Cleared
0
Denied
FDA 510(k) cleared devices by 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