Anx Robotica Corporation - FDA 510(k) Cleared Devices
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) cleared devices by 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