DUCKWORTH & KENT, LTD.

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
80218171000231766DUCKWORTH & KENT, LTD.1N2026-01-017 MARQUIS BUSINESS CENTRE ROYSTON RD. BALDOCK Hertfordshire GB SG7 6XL

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
406351816506985K081382DUCKWORTH & KENT, LTD., IMPLANTATION SYSTEM, MODEL DK7786KYB2008-10-23
406351200544726K072985DUCKWORTH & KENT LTD INJECTOR, MODEL: DK7797-2KYB2008-06-20
406351952716955K053176DUCKWORTH & KENT LTD CARTRIDGE LENS DELIVERY SYSTEM, MODEL DK7797MSS2006-01-30
406351899553781K042478CAPSULE TENSION RING INSERTER, MODEL 7-810NCE2004-12-28
406351032784013
406351042473955
406351055859309
406351075332494
406351076819556
406351209345450
406351323064103
406351434220882
406351467795732
406351579107556
406351587866214
406351651173046
406351707537501
406351755547323
406351827359624
406351870131927
406351888201389
406352043967378

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
KYB22008-10-23
MSS12006-01-30
NCE12004-12-28

PMN#