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L&K Biomed

South Korea·KR-MF-000033200

Last updated June 8, 2026

What L&K Biomed makes

L&K Biomed manufactures spinal bone screws, non-bioabsorbable, and bone-screw internal spinal fixation system connectors. Their product line includes the BluEX Cervical Expandable Cage System and the AccelFix Spinal Fixation System, which are used for spinal fixation and cage procedures.

The company's devices are classified as Class II and Class IIb and are listed in the EUDAMED and FDA 510(k) registries. L&K Biomed 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 medical devices does L&K Biomed manufacture?

L&K Biomed specializes in spinal bone screws that are non-bioabsorbable and bone-screw internal spinal fixation system connectors. Their product line includes the BluEX Cervical Expandable Cage System and the AccelFix Spinal Fixation System, which are used for spinal fixation and cage procedures.

Where is L&K Biomed based?

L&K Biomed is based in South Korea, as indicated by the country code KR in their device data. The company operates from this location to manufacture and distribute their spinal fixation devices.

Which regulatory registries list L&K Biomed's devices?

L&K Biomed's devices are listed in the EUDAMED and FDA 510(k) registries. These are regulatory databases that track medical devices in the European Union and United States markets respectively.

How are L&K Biomed's devices classified?

L&K Biomed's devices are classified as Class II and Class IIb. These classifications indicate the level of regulatory control required, with Class IIb typically representing higher risk devices that need more stringent regulatory oversight.

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

Information

Country: South Korea
Address: 16-25, Dongbaekjungang-ro 16beon-gil, Giheung-gu, Yongin-si, Gyeonggi-do, South Korea
Website: lnkbiomed.com
LinkedIn: —
Facebook: —
Email: [email protected]
Phone: —
PRRC Contact: Miyoung Koh
EUDAMED SRN: KR-MF-000033200
FDA FEI Number: —
DUNS Number: —

Catalogue (30302)

Page 12 of 500

Device	Model / Reference	Registries	Class	Status
LnK Lumbar Interbody Fusion Cage System	3870-5013	FDA UDI	Class II	Active
CastleLoc Spinal Fixation System/LnK Basic Spinal Fixation System	1521-8040	FDA UDI	Class II	Active
PathLoc-L MIS Spinal System, LnK MIS Spinal System	2730-5555	FDA UDI	Class II	Active
LnK Spinal Fixation System	1071-63360	FDA UDI	Class II	Active
LnK Spinal Fixation System	1845-6265	FDA UDI	Class II	Active
AccelFix Lumbar Expandable Cage System	L6518-1200	FDA UDI	Class II	Active
LnK/PathLoc-L MIS Spinal System	2727-6550S	FDA UDI	Class II	Active
LnK Spinal Fixation System	1071-55370	FDA UDI	Class II	Active
LnK MIS Spinal System	2609-6535	FDA UDI	Class II	Active
LnK Cervical Interbody Fusion Cage System	5105-1517	FDA UDI	Class II	Active
LnK MIS Spinal System	2510-55100	FDA UDI	Class II	Active
LnK Spinal Fixation System	1071-60570	FDA UDI	Class II	Active
LnK Spinal Fixation System	1321-8050	FDA UDI	Class II	Active
LnK Spinal Fixation System	1087-50130	FDA UDI	Class II	Active
LnK Spinal Fixation System	1351-65120	FDA UDI	Class II	Active
AccelFix Spinal Fixation System	8113-6555	FDA UDI	Class II	Active
AccelFix Lumbar Plate System	7301-6040S	FDA UDI	Class II	Active
LnK/PathLoc-L MIS Spinal System	2810-6545S	FDA UDI	Class II	Active
LnK Spinal Fixation System	1421-7590	FDA UDI	Class II	Active
LnK Spinal Fixation System	1411-80140	FDA UDI	Class II	Active
LnK Spinal Fixation System	1332-85145	FDA UDI	Class II	Active
AccelFix Spinal Fixation System	8122-75145	FDA UDI	Class II	Active
AccelFix Lumbar Expandable Cage System	L6518-1009	FDA UDI	Class II	Active
AccelFix Lumbar Expandable Cage System	L5524-1006	FDA UDI	Class II	Active
AccelFix Spinal Fixation System	8112-6525	FDA UDI	Class II	Active
LnK Lumbar Interbody Fusion Cage System	3832-5008	FDA UDI	Class II	Active
AccelFix Spinal Fixation System	8111-6020	FDA UDI	Class II	Active
PathLoc-C Posterior Cervical Fixation System	6319-3526	FDA UDI	Class II	Active
CastleLoc Spinal Fixation System/LnK Basic Spinal Fixation System	1551-4560	FDA UDI	Class II	Active
CastleLoc Spinal Fixation System/LnK Basic Spinal Fixation System	1532-7565	FDA UDI	Class II	Active
LnK Lumbar Interbody Fusion Cage System/PathLoc-LC Lateral Cage System	3856-6010S	FDA UDI	Class II	Active
LnK Spinal Fixation System	1451-6555	FDA UDI	Class II	Active
LnK Spinal Fixation System	1351-6575	FDA UDI	Class II	Active
LnK MIS Spinal System	2520-5580	FDA UDI	Class II	Active
LnK Spinal Fixation System	1412-65105	FDA UDI	Class II	Active
AccelFix Spinal Fixation System	2512-5540S	FDA UDI	Class II	Active
LnK/PathLoc-L MIS Spinal System	2709-6535S	FDA UDI	Class II	Active
LnK Spinal Fixation System	1052-60490	FDA UDI	Class II	Active
LnK Spinal Fixation System	1047-1025	FDA UDI	Class II	Active
AccelFix Spinal Fixation System	8124-75110	FDA UDI	Class II	Active
CastleLoc-S Posterior Cervical Fixation System/LnK Posterior Cervical Fixation S	6111-4022	FDA UDI	Class II	Active
CastleLoc Spinal Fixation System/LnK Basic Spinal Fixation System	1532-7025	FDA UDI	Class II	Active
LnK Spinal Fixation System	1351-6040	FDA UDI	Class II	Active
LnK Spinal Fixation System	1151-4520	FDA UDI	Class II	Active
AccelFix Lumbar Expandable Cage System	L6018-1012	FDA UDI	Class II	Active
LnK Spinal Fixation System	1431-7030	FDA UDI	Class II	Active
LnK Spinal Fixation System	1332-8580	FDA UDI	Class II	Active
AccelFix Spinal Fixation System	8122-6555	FDA UDI	Class II	Active
AccelFix Spinal Fixation System	8123-6545	FDA UDI	Class II	Active
CastleLoc-P Anterior Cervical Plate System	6608-3512S	FDA UDI	Class II	Active

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