Anx Robotica Corp is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Anx Robotica Corp - FDA 510(k) Cleared Devices
Recent clearances: NaviCam Xpress Stomach Capsule Endoscope System (NaviCam Xpress Stomach System) with NaviCam Stomach Capsule/Tether (NaviCam Xpress Stomach System with NaviCam Capsule/Tether), NaviCam Xpress Stomach System, NaviCam Xpress System, NaviCam Capsule Endoscope System with NaviCam Stomach Capsule and NaviCam Tether, NaviCam Xpress Stomach Capsule Endoscope System (NaviCam Xpress Stomach System) with NaviCam Stomach Capsule and NaviCam Tether
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.
510(k) submissions have been managed by Emergo Global Consulting, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - 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