DUCKWORTH & KENT, LTD., IMPLANTATION SYSTEM, MODEL DK7786— 510(k) K081382

Substantially Equivalent

Duckworth & Kent, Ltd.

FDA 510(k) clearance K081382 for DUCKWORTH & KENT, LTD., IMPLANTATION SYSTEM, MODEL DK7786, Substantially Equivalent on 2008-10-23. Applicant: Duckworth & Kent, Ltd..

Clearance details

Applicant: Duckworth & Kent, Ltd.
Product code: Code KYB
Advisory panel: Ophthalmic
Date received: 2008-05-16
Decision date: 2008-10-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Baldock, Hertfordshire, GB

Download summary PDF View on FDA.gov ↗

Adverse events under product code KYB

product code KYB

Injury: 218
Malfunction: 1,989
Other: 1
Total: 2,208

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.