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DUCKWORTH AND KENT LIMITED

US

Last updated May 24, 2026

What DUCKWORTH AND KENT LIMITED makes

Duckworth and Kent Limited manufactures reusable ophthalmic surgical instruments, including scleral incision positioning frames, irrigation/infusion/aspiration cannulas, and various forceps for handling implants and surgical devices. Their portfolio also covers specialized tools like corneal markers, scleral expansion implant implantation tools, and reusable surgical screwdrivers, all designed for precision in eye surgery. The company produces non-illuminating cannulas and reusable probes for ophthalmic procedures, ensuring compatibility with surgical workflows.

All devices from Duckworth and Kent Limited fall under Class I regulatory classification in the US, with listings maintained in the FDA’s UDI (Unique Device Identification) database. The company is based in the United States, adhering to domestic regulatory requirements for medical device authorization.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What types of medical devices does Duckworth and Kent Limited manufacture?

Duckworth and Kent Limited specializes in reusable ophthalmic surgical instruments. Their portfolio includes devices like scleral incision positioning frames, irrigation/infusion/aspiration cannulas (non-illuminating), corneal markers, and various forceps for handling implants and surgical tools. They also produce specialized tools such as scleral expansion implant implantation tools and reusable surgical screwdrivers, all designed for precision in eye surgery procedures.

Where is Duckworth and Kent Limited based, and does this affect their regulatory requirements?

Duckworth and Kent Limited is based in the United States. Since they operate domestically, their devices must comply with U.S. regulatory requirements for medical device authorization. The company’s products are classified under Class I in the US, which is the lowest risk category, and their listings are maintained in the FDA’s UDI (Unique Device Identification) database.

Which regulatory registries or databases list Duckworth and Kent Limited’s devices?

Duckworth and Kent Limited’s devices are listed in the FDA’s UDI (Unique Device Identification) database. This registry ensures traceability and transparency of their Class I medical devices, which are primarily used in ophthalmic surgery. The UDI system helps track authorized devices for compliance and market surveillance purposes.

How are Duckworth and Kent Limited’s devices classified in the US regulatory system?

All of Duckworth and Kent Limited’s devices fall under Class I classification in the US regulatory system. This classification is assigned based on risk assessment—Class I devices are generally considered the lowest risk and often involve minimal potential harm to patients. Since these instruments are reusable ophthalmic tools, their design and intended use align with the criteria for this classification.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
US
Address
—
LinkedIn
—
Facebook
—
Phone
+441462893254
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
—
DUNS Number
217182583

Catalogue (98)

Page 2 of 2
DeviceModel / ReferenceRegistriesClassStatus
Duckworth & Kent 8-604
FDA UDI
Class IUnknown
Duckworth & Kent 8-011
FDA UDI
Class IActive
Duckworth & Kent 2-878-1
FDA UDI
Class IUnknown
Duckworth & Kent 7-810
FDA UDI
Class IUnknown
Duckworth & Kent 6-181
FDA UDI
Class IUnknown
Duckworth & Kent 6-075
FDA UDI
Class IUnknown
Duckworth & Kent 4-620-4
FDA UDI
Class IUnknown
Duckworth & Kent 4-430
FDA UDI
Class IUnknown
Duckworth & Kent 6-652
FDA UDI
Class IActive
Duckworth & Kent 6-105-1
FDA UDI
Class IUnknown
Duckworth & Kent 6-135-1
FDA UDI
Class IUnknown
Duckworth & Kent T7020
FDA UDI
Class IUnknown
Duckworth & Kent 9-855
FDA UDI
Class IUnknown
Duckworth & Kent 6-083-5
FDA UDI
Class IUnknown
Duckworth & Kent 1-842N
FDA UDI
Class IUnknown
Duckworth & Kent 6-675
FDA UDI
Class IUnknown
Duckworth & Kent 9-687
FDA UDI
Class IUnknown
Duckworth & Kent 33-222
FDA UDI
Class IUnknown
Duckworth & Kent 1-700
FDA UDI
Class IUnknown
Duckworth & Kent 9-544-4
FDA UDI
Class IUnknown
Duckworth & Kent 2-195-1
FDA UDI
Class IUnknown
Duckworth & Kent 1-841
FDA UDI
Class IUnknown
Duckworth & Kent 6-086-4
FDA UDI
Class IUnknown
Duckworth & Kent 9-518-3
FDA UDI
Class IUnknown
Duckworth & Kent 2-731
FDA UDI
Class IActive
Duckworth & Kent 9-779
FDA UDI
Class IUnknown
Duckworth & Kent 1-120
FDA UDI
Class IUnknown
Duckworth & Kent 9-854R
FDA UDI
Class IUnknown
Duckworth & Kent 6-194-2
FDA UDI
Class IActive
Duckworth & Kent 8-652S
FDA UDI
Class IUnknown
Duckworth & Kent 4-620-3
FDA UDI
Class IUnknown
Duckworth & Kent 9-566
FDA UDI
Class IUnknown
Duckworth & Kent 6-615-1
FDA UDI
Class IUnknown
Duckworth & Kent 6-645
FDA UDI
Class IUnknown
Duckworth & Kent 9-687-3
FDA UDI
Class IUnknown
Duckworth & Kent 2-877N
FDA UDI
Class IUnknown
Duckworth & Kent 8-652-1S
FDA UDI
Class IUnknown
Duckworth & Kent 2-716GNR8-3
FDA UDI
Class IUnknown
Duckworth & Kent 6-912
FDA UDI
Class IUnknown
Duckworth & Kent 6-090-7
FDA UDI
Class IActive
Duckworth & Kent 6-130
FDA UDI
Class IUnknown
Duckworth & Kent 2-195
FDA UDI
Class IUnknown
Duckworth & Kent 9-864-1
FDA UDI
Class IActive
Duckworth & Kent 9-840-3
FDA UDI
Class IUnknown
Duckworth & Kent 9-687-2
FDA UDI
Class IUnknown
Duckworth & Kent 9-589
FDA UDI
Class IUnknown
Duckworth & Kent 6-629
FDA UDI
Class IUnknown
Duckworth & Kent 9-581F
FDA UDI
Class IUnknown

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