Anx Robotica Corporation is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
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
Anx Robotica Corporation has 3 FDA 510(k) cleared medical devices. Based in Plano, US.
Latest FDA clearance: May 2025. Active since 2023. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Anx Robotica Corporation Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Anx Robotica Corporation
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