Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Duckworth & Kent, Ltd. — Predicate Candidate Screening
6 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
160 daysmedian FDA review time
300 days90th percentile
6clearances measured
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K081382 | DUCKWORTH & KENT, LTD., IMPLANTATION SYSTEM, MODEL DK7786 | Duckworth & Kent, Ltd. | 2008-10-23 | 160 | 0 |
| K072985 | DUCKWORTH & KENT LTD INJECTOR, MODEL: DK7797-2 | Duckworth & Kent, Ltd. | 2008-06-20 | 241 | 0 |
| K060995 | DUCKWORTH & KENT LTD LENS DELIVERY SYSTEM, MODEL DK7788 | Duckworth & Kent, Ltd. | 2006-05-22 | 41 | 0 |
| K053176 | DUCKWORTH & KENT LTD CARTRIDGE LENS DELIVERY SYSTEM, MODEL D | Duckworth & Kent, Ltd. | 2006-01-30 | 77 | 0 |
| K042478 | CAPSULE TENSION RING INSERTER, MODEL 7-810 | Duckworth & Kent, Ltd. | 2004-12-28 | 106 | 0 |
| K024072 | DUCKWORTH & KENT LTD LENS DELIVERY SYSTEM | Duckworth & Kent, Ltd. | 2003-10-06 | 300 | 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