Anx Robotica Corp - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Anx Robotica Corp has 6 FDA 510(k) cleared medical devices. Based in Plano, US.
Latest FDA clearance: Jul 2024. Active since 2019. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Anx Robotica Corp Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Anx Robotica Corp
6 devices
Cleared
Jul 31, 2024
NaviCam Xpress Stomach Capsule Endoscope System (NaviCam Xpress Stomach...
Gastroenterology & Urology
29d
Cleared
Apr 13, 2023
NaviCam Xpress Stomach System, NaviCam Xpress System
Gastroenterology & Urology
31d
Cleared
Nov 22, 2022
NaviCam Capsule Endoscope System with NaviCam Stomach Capsule and NaviCam...
Gastroenterology & Urology
172d
Cleared
May 04, 2021
NaviCam Xpress Stomach System
Gastroenterology & Urology
188d
Cleared
May 21, 2020
IntraMarX 3D Radiopaque Marker
Gastroenterology & Urology
27d
Cleared
Dec 18, 2019
IntraMarX Radiopaque Markers
Gastroenterology & Urology
238d