Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
NLL · 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) |
|---|---|---|---|---|---|
| K070930 | REPROCESSED AUTOSUTURE GIA ENDOSCOPIC STAPLERS | Sterilmed, Inc. | 2007-10-18 | 198 | 0 |
| K070859 | REPROCESSED ETHICON ETS ENDOSCOPIC LINEAR CUTTERS | Sterilmed, Inc. | 2007-09-12 | 168 | 0 |
| K033578 | REPROCESSED RELOADABLE CUTTERS, STAPLERS, AND APPLIERS | Clearmedical, Inc. | 2005-07-11 | 606 | 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