Company ยท US
Anx Robotica Corp
FDA 510(k) clearances and medical device recalls filed under this name, 2019 to 2025. Name variants (Inc, Corp, punctuation) are merged.
10510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| May 21, 2025 | K250493 | MotiliCap GI Monitoring System Anx Robotica Corporation | NYV |
| Jul 31, 2024 | K241934 | NaviCam Xpress Stomach Capsule Endoscope System (NaviCam Xpress Stomach System) with NaviCam Stomach Capsule/Tether (Nav Anx Robotica Corp | QKZ |
| Jan 5, 2024 | K233229 | NaviCam Small Bowel Capsule Endoscopy System with NaviCam SB Capsule and NaviCam Tether Anx Robotica Corporation | NEZ |
| Oct 3, 2023 | K231960 | NaviCam Xpress Stomach Capsule Endoscope System (NaviCam Xpress Stomach System) with NaviCam Capsule and NaviCam Tether Anx Robotica Corporation | QKZ |
| Apr 13, 2023 | K230694 | NaviCam Xpress Stomach System, NaviCam Xpress System Anx Robotica Corp | QKZ |
| Nov 22, 2022 | K221608 | NaviCam Capsule Endoscope System with NaviCam Stomach Capsule and NaviCam Tether, NaviCam Xpress Stomach Capsule Endosco Anx Robotica Corp | QKZ |
| May 4, 2021 | K203192 | NaviCam Xpress Stomach System Anx Robotica Corp | QKZ |
| May 22, 2020 | DEN190037 | NaviCam Capsule Endoscope System with NaviCam Stomach Capsule Anx Robotica, Inc. | QKZ |
| May 21, 2020 | K201106 | IntraMarX 3D Radiopaque Marker Anx Robotica Corp | FFX |
| Dec 18, 2019 | K191087 | IntraMarX Radiopaque Markers Anx Robotica Corp | FFX |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||