Anx Robotica Corporation
FDA 510(k) & PMA Approved Devices — 3 products
Total Devices3
Categories3
Latest FDA decision2025-05-21
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K250493 | MotiliCap GI Monitoring System | NYV | 2025-05-21 | View |
| 510(k) | K233229 | NaviCam Small Bowel Capsule Endoscopy System with NaviCam SB Capsule and NaviCam Tether | NEZ | 2024-01-05 | View |
| 510(k) | K231960 | NaviCam Xpress Stomach Capsule Endoscope System (NaviCam Xpress Stomach System) with NaviCam Capsule and NaviCam Tether | QKZ | 2023-10-03 | View |
No matching devices.
Related Clinical Trials
NCT04605302Comparative Study of MCCE With/Without Tether vs Conventional Upper Endoscopy in Patients With Upper Abdominal SymptomsCOMPLETEDNCT07633847A Post Market Trial Assessing the Accuracy of Normal Mode Reading vs. ProScan Reading With the NaviCam SB System. This is a Comparison of Retrospectively Obtained Capsule Endoscopy Videos With a New AI Reading Tool; no New Interventions Will be Completed.NOT_YET_RECRUITINGNCT07649720NaviCam Patency Capsule to Verify Gastrointestinal PatencyNOT_YET_RECRUITING