Predicate Research Report · generated 2026-08-23 · Print / save as PDF · Save to account
PWI · Predicate Candidate Screening
2 FDA 510(k) clearances under this product code; the 50 most recent screened below.
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K173527 | Digitex Delivery Device | Coloplast A/S | 2018-02-12 | 90 | 0 |
| K172060 | Capio SLIM Suture Capturing Device | Boston Scientific Corporation | 2017-11-03 | 119 | 4 |
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