Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
QQC · Predicate Candidate Screening
3 FDA 510(k) clearances under this product code; the 50 most recent screened below.
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K243520 | Bullsai Confirm | Turing Medical Technologies, Inc. | 2025-03-28 | 135 | 0 |
| K213930 | Brainlab Elements Guide XT, Guide 3.0 | Brainlab AG | 2022-04-19 | 124 | 0 |
| DEN210003 | SureTune4 Software | Medtronic Neuromodulation | 2021-08-23 | 201 | 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