Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Anx Robotica Corporation · Predicate Candidate Screening
3 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K250493 | MotiliCap GI Monitoring System | Anx Robotica Corporation | 2025-05-21 | 90 | 0 |
| K233229 | NaviCam Small Bowel Capsule Endoscopy System with NaviCam SB | Anx Robotica Corporation | 2024-01-05 | 99 | 0 |
| K231960 | NaviCam Xpress Stomach Capsule Endoscope System (NaviCam Xpr | Anx Robotica Corporation | 2023-10-03 | 92 | 0 |
Methodology
Recall counts reflect FDA recall records explicitly referencing each K-number; FDA links recalls to K-numbers inconsistently, so 0 means "none found in FDA records," not "never recalled." Data: FDA openFDA, refreshed weekly. Verify decisions of consequence against the primary source. Full candidate set and CSV export: atlasbyauro.com.
Prepared with Atlas
Predicate research, review-time statistics and recall monitoring for 510(k) teams: atlasbyauro.com/fda