Predicate Research Report · generated 2026-08-23 · Print / save as PDF · Save to account
KBD · 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) |
|---|---|---|---|---|---|
| K851763 | 13-320,13-330 TWO TYPES NAZAL SCISSORS-HEYMAN,BECK | Artiberia | 1985-06-11 | 47 | 0 |
| K822524 | EAR SPOON | Kelleher Corp. | 1982-09-09 | 17 | 0 |
| K791124 | SURGICAL SCISSORS | Xomed, Inc. | 1979-06-27 | 12 | 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