Anx Robotica Corp
Anx Robotica Corp appears in FDA public data with 0 recalls, 7 510(k) clearances, 2 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on July 31, 2024.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 7
- Inspections
- 2
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K241934 | NaviCam Xpress Stomach Capsule Endoscope System (NaviCam Xpress Stomach System) with NaviCam Stomach | July 31, 2024 |
| K230694 | NaviCam Xpress Stomach System, NaviCam Xpress System | April 13, 2023 |
| K221608 | NaviCam Capsule Endoscope System with NaviCam Stomach Capsule and NaviCam Tether, NaviCam Xpress Sto | November 22, 2022 |
| K203192 | NaviCam Xpress Stomach System | May 4, 2021 |
| DEN190037 | NaviCam Capsule Endoscope System with NaviCam Stomach Capsule | May 22, 2020 |
| K201106 | IntraMarX 3D Radiopaque Marker | May 21, 2020 |
| K191087 | IntraMarX Radiopaque Markers | December 18, 2019 |