Data / Medical devices / United Kingdom / Duckworth & Kent, Ltd.

Duckworth & Kent, Ltd.: FDA-registered device maker in BALDOCK Hertfordshire, United Kingdom, 3 510(k) clearances

Name: Duckworth & Kent, Ltd. FDA registration, clearances, approvals and recalls
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

Duckworth & Kent, Ltd. is registered with the FDA (registration 8021817) in BALDOCK Hertfordshire, United Kingdom. It lists 20 device types. The FDA files 3 510(k) clearances under its listings, the newest dated October 23, 2008. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number: 8021817
FEI number: 1000231766
Address: 7 Marquis Business Centre Royston RD., BALDOCK Hertfordshire, United Kingdom, SG7 6XL
Owner or operator: Duckworth & Kent Ltd (8021817)
Roles: Manufacturer
First device listed: October 19, 1995
Registered through: 2026
Brand names listed: & KENT RETRACTORS, BLOOMBERG TRABECULOTOME SET, BRANDS), Capsule Tension Ring Inserter, DS), DUCKWORTH, DUCKWORTH & KENT TREPHINES, DUKWORTH and more

Devices it lists

Device	Product code	Class	Role	Source
Caliper, Ophthalmic	HOE	1	Manufacturer	accessdata.fda.gov
Cannula, Ophthalmic	HMX	1	Manufacturer	accessdata.fda.gov
Clamp, Eyelid, Ophthalmic	HOD	1	Manufacturer	accessdata.fda.gov
Curette, Ophthalmic	HNZ	1	Manufacturer	accessdata.fda.gov
Depressor, Orbital	HNX	1	Manufacturer	accessdata.fda.gov
Forceps, Ophthalmic	HNR	1	Manufacturer	accessdata.fda.gov
Hook, Ophthalmic	HNQ	1	Manufacturer	accessdata.fda.gov
Injector, Capsular Tension Ring	NCE	1	Manufacturer	accessdata.fda.gov
Knife, Ophthalmic	HNN	1	Manufacturer	accessdata.fda.gov
Lens, Guide, Intraocular	KYB	1	Manufacturer	accessdata.fda.gov
Marker, Ocular	HMR	1	Manufacturer	accessdata.fda.gov
Needle, Ophthalmic Suturing	HNM	1	Manufacturer	accessdata.fda.gov
Retractor, Ophthalmic	HNI	1	Manufacturer	accessdata.fda.gov
Ring, Ophthalmic (Flieringa)	HNH	1	Manufacturer	accessdata.fda.gov
Scissors, Ophthalmic	HNF	1	Manufacturer	accessdata.fda.gov
Spatula, Ophthalmic	HND	1	Manufacturer	accessdata.fda.gov
Trabeculotome	HMZ	1	Manufacturer	accessdata.fda.gov
Tray, Surgical, Instrument	FSM	1	Manufacturer	accessdata.fda.gov
Trephine, Manual, Ophthalmic	HRH	1	Manufacturer	accessdata.fda.gov
Wrench	HXC	1	Manufacturer	accessdata.fda.gov

510(k) clearances

The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.

Decided	510(k) number	Device	Product code	Decision	Applicant	Source
October 23, 2008	K081382	DUCKWORTH & KENT, LTD., IMPLANTATION SYSTEM, MODEL DK7786	KYB	Substantially Equivalent	Duckworth & Kent, Ltd.	accessdata.fda.gov
June 20, 2008	K072985	DUCKWORTH & KENT LTD INJECTOR, MODEL: DK7797-2	KYB	Substantially Equivalent	Duckworth & Kent, Ltd.	accessdata.fda.gov
December 28, 2004	K042478	CAPSULE TENSION RING INSERTER, MODEL 7-810	NCE	Substantially Equivalent	Duckworth & Kent, Ltd.	accessdata.fda.gov

Compare with other makers

Updated October 23, 2008. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.