Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
LRZ · 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) |
|---|---|---|---|---|---|
| K896589 | MANUAL SURGICAL INSTRUMENTS FOR TITAMED ANTWERP | Optik | 1989-12-27 | 36 | 0 |
| K872490 | 1.1 SCREWDRIVERS | Micro-Aire Surgical Instruments, Inc. | 1987-07-23 | 30 | 0 |
| K872387 | STANDARD SCREW DRIVER | Med-Tool, Inc. | 1987-07-16 | 27 | 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