Duckworth & Kent, Ltd.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
6
Inspections
1
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K081382DUCKWORTH & KENT, LTD., IMPLANTATION SYSTEM, MODEL DK7786October 23, 2008
K072985DUCKWORTH & KENT LTD INJECTOR, MODEL: DK7797-2June 20, 2008
K060995DUCKWORTH & KENT LTD LENS DELIVERY SYSTEM, MODEL DK7788May 22, 2006
K053176DUCKWORTH & KENT LTD CARTRIDGE LENS DELIVERY SYSTEM, MODEL DK7797January 30, 2006
K042478CAPSULE TENSION RING INSERTER, MODEL 7-810December 28, 2004
K024072DUCKWORTH & KENT LTD LENS DELIVERY SYSTEMOctober 6, 2003