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Duk-In Co., Ltd.

South Korea·KR-MF-000026961

Last updated September 18, 2026

What Duk-In Co., Ltd. makes

Duk-In Co., Ltd. manufactures orthopedic splints and casts, including models such as the Duk-In N-Splint, Duk-In S-Splint, Duk-In Splint, Duk-In Lite 'S', and Duk-In Cast. These devices are designed for immobilizing and supporting limbs, aiding in the recovery and stabilization of fractures or injuries.

The company’s products are classified as Class I medical devices and are registered in the EU’s eudamed database. Duk-In Co., Ltd. is based in South Korea.

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 Duk-In Co., Ltd. manufacture?

Duk-In Co., Ltd. specializes in orthopedic devices, specifically designing and producing splints and casts. Their product line includes models like the Duk-In N-Splint, Duk-In S-Splint, Duk-In Splint, Duk-In Lite 'S', and Duk-In Cast. These devices are intended for immobilizing and supporting limbs during the recovery and stabilization of fractures or injuries.

Where is Duk-In Co., Ltd. based?

Duk-In Co., Ltd. is headquartered in South Korea. The company’s location in South Korea influences its regulatory and manufacturing operations, though its devices may be distributed globally depending on market demand and compliance requirements.

Which regulatory registries list Duk-In Co., Ltd.’s devices?

Duk-In Co., Ltd.’s devices are registered in the eudamed database, which is the European Union’s central registry for medical devices. This registration reflects compliance with EU regulatory requirements for Class I devices, though it does not imply approval or clearance—only that the devices are listed for transparency and traceability.

How are Duk-In Co., Ltd.’s devices classified under medical device regulations?

All of Duk-In Co., Ltd.’s devices fall under Class I classification. This classification is typically assigned to low-risk devices like orthopedic splints and casts, which pose minimal risk to patients when used as intended. Class I devices often require less stringent regulatory oversight compared to higher-risk categories.

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

Information

Country
South Korea
Address
134, Hwanamgongdan-ro, Seosin-Myeon, Hwaseong-si, Gyeonggi-do, South Korea
Website
www.dukin.com
LinkedIn
—
Facebook
—
Phone
—
PRRC Contact
Jiwoong Choi
EUDAMED SRN
KR-MF-000026961
FDA FEI Number
—
DUNS Number
—

Catalogue (22)

DeviceModel / ReferenceRegistriesClassStatus
Duk-In N-Splint S4210
EUDAMED
Class IActive
Duk-In S-Splint S3210
EUDAMED
Class IActive
Duk-In Splint S3855
EUDAMED
Class IActive
Duk-In S-Splint S3645
EUDAMED
Class IActive
Duk-In S-Splint S4312
EUDAMED
Class IActive
Duk-In Lite 'S' L4144
EUDAMED
Class IActive
Duk-In N-Splint S4335
EUDAMED
Class IActive
Duk-In N-Splint S4855
EUDAMED
Class IActive
Duk-In N-Splint S4865
EUDAMED
Class IActive
Duk-In N-Splint S4430
EUDAMED
Class IActive
Duk-In Cast C1083
EUDAMED
Class IActive
Duk-In Cast C1033
EUDAMED
Class IActive
Duk-In Slint S3545
EUDAMED
Class IActive
Duk-In Cast C1043
EUDAMED
Class IActive
Duk-In Cast C1063
EUDAMED
Class IActive
Duk-In S-Splint S3835
EUDAMED
Class IActive
Duk-In S-Splint S3335
EUDAMED
Class IActive
Duk-In S-Splint S3415
EUDAMED
Class IActive
Duk-In N-Splint S4630
EUDAMED
Class IActive
Duk-In Lite 'S' L4124
EUDAMED
Class IActive
Duk-In S-Splint S3825
EUDAMED
Class IActive
Duk-In N-Splint S4545
EUDAMED
Class IActive

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