Medical Device Manufacturer · US , Plano , TX

Anx Robotica Corporation - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 2023

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
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