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Sign in to claim this brandDuk-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
- —
- —
- [email protected]
- Phone
- —
- PRRC Contact
- Jiwoong Choi
- EUDAMED SRN
- KR-MF-000026961
- FDA FEI Number
- —
- DUNS Number
- —
Catalogue (22)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Duk-In N-Splint | S4210 | EUDAMED | Class I | Active |
| Duk-In S-Splint | S3210 | EUDAMED | Class I | Active |
| Duk-In Splint | S3855 | EUDAMED | Class I | Active |
| Duk-In S-Splint | S3645 | EUDAMED | Class I | Active |
| Duk-In S-Splint | S4312 | EUDAMED | Class I | Active |
| Duk-In Lite 'S' | L4144 | EUDAMED | Class I | Active |
| Duk-In N-Splint | S4335 | EUDAMED | Class I | Active |
| Duk-In N-Splint | S4855 | EUDAMED | Class I | Active |
| Duk-In N-Splint | S4865 | EUDAMED | Class I | Active |
| Duk-In N-Splint | S4430 | EUDAMED | Class I | Active |
| Duk-In Cast | C1083 | EUDAMED | Class I | Active |
| Duk-In Cast | C1033 | EUDAMED | Class I | Active |
| Duk-In Slint | S3545 | EUDAMED | Class I | Active |
| Duk-In Cast | C1043 | EUDAMED | Class I | Active |
| Duk-In Cast | C1063 | EUDAMED | Class I | Active |
| Duk-In S-Splint | S3835 | EUDAMED | Class I | Active |
| Duk-In S-Splint | S3335 | EUDAMED | Class I | Active |
| Duk-In S-Splint | S3415 | EUDAMED | Class I | Active |
| Duk-In N-Splint | S4630 | EUDAMED | Class I | Active |
| Duk-In Lite 'S' | L4124 | EUDAMED | Class I | Active |
| Duk-In S-Splint | S3825 | EUDAMED | Class I | Active |
| Duk-In N-Splint | S4545 | EUDAMED | Class I | Active |
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