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CORELINK LLC

Last updated May 24, 2026

What CORELINK LLC makes

CoreLink LLC manufactures spinal fixation devices, including non-sterile and sterile bone-screw systems for internal spinal stabilization, non-bioabsorbable spinal plates, and metallic and polymeric interbody fusion cages. Their portfolio also covers orthopaedic bone screws designed for non-sliding applications, as well as lateral screws and 3D lateral cages for spinal support.

All listed devices fall under FDA Class II regulation and are recorded in the FDA’s Unique Device Identifier (UDI) database. The company is based in the United States.

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 CoreLink LLC manufacture?

CoreLink LLC specializes in spinal fixation devices. Their portfolio includes bone-screw systems for internal spinal stabilization (both non-sterile and sterile), non-bioabsorbable spinal plates, metallic and polymeric interbody fusion cages, and orthopaedic bone screws designed for non-sliding applications. These devices are primarily used to support and stabilize the spine during surgical procedures.

Where is CoreLink LLC based?

CoreLink LLC is based in the United States. The company’s headquarters and operations are located within the country, though specific regional offices or manufacturing sites may vary.

Which regulatory registries list CoreLink LLC’s devices?

CoreLink LLC’s devices are recorded in the FDA’s Unique Device Identifier (UDI) database. This registry tracks Class II devices, which include all of CoreLink’s listed products, ensuring traceability and compliance with U.S. regulatory requirements.

How are CoreLink LLC’s devices classified under FDA regulations?

CoreLink LLC’s devices fall under FDA Class II classification. This classification applies to moderate-risk medical devices that require special controls to ensure safety and effectiveness, such as spinal fixation systems and interbody fusion cages.

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

Information

Country: US
Address: —
Website: corelinksurgical.com
LinkedIn: —
Facebook: —
Email: [email protected]
Phone: +1(314)863-5401
PRRC Contact: —
EUDAMED SRN: —
FDA FEI Number: —
DUNS Number: 064191453

Catalogue (3588)

Page 54 of 72

Device	Model / Reference	Registries	Class	Status
TIGER Spine System	77545-60	FDA UDI	Class II	Active
CoreLink 3D Lateral Cage	3LL1860-3016	FDA UDI	Class II	Active
TIGER Spine OCT System	R3512-080	FDA UDI	Class II	Active
TIGER Spine System	60085-30	FDA UDI	Class II	Active
TIGER Spine System	61065-30	FDA UDI	Class II	Active
TIGER Spine System	55845-45	FDA UDI	Class II	Active
TIGER Spine System	55495-100	FDA UDI	Class II	Active
TIGER Spine OCT System	35835-26	FDA UDI	Class II	Active
FOUNDATION System	MAT1313	FDA UDI	Class II	Active
TIGER Spine System	77605-120	FDA UDI	Class II	Active
FOUNDATION System	840855-13	FDA UDI	Class II	Active
TIGER Spine OCT System	35845-20	FDA UDI	Class II	Active
TIGER Spine OCT System	35945-20	FDA UDI	Class II	Active
CoreLink 3D Lateral Cage	3LL1855-0014	FDA UDI	Class II	Active
TIGER Spine System	55085-50	FDA UDI	Class II	Active
ANODYNE Plate System	20140-14	FDA UDI	Class II	Active
TIGER Spine OCT System	R3510-020	FDA UDI	Class II	Active
CoreLink Foundation 3D ALIF Stand-Alone Cage	3AS2735-0820	FDA UDI	Class II	Active
TIGER Spine System	77855-50	FDA UDI	Class II	Active
CoreLink 3D Lateral Cage	3LL1855-2012	FDA UDI	Class II	Active
TIGER Spine System	55185-70	FDA UDI	Class II	Active
FOUNDATION System	840045-08	FDA UDI	Class II	Active
TIGER Spine System	61075-60	FDA UDI	Class II	Active
FOUNDATION System	870025-09	FDA UDI	Class II	Active
TIGER Spine System	55075-60	FDA UDI	Class II	Active
ANODYNE Plate System	21246-14	FDA UDI	Class II	Active
TIGER Spine OCT System	35035-30	FDA UDI	Class II	Active
TIGER Spine System	77365-35	FDA UDI	Class II	Active
TIGER Spine OCT System	35935-38	FDA UDI	Class II	Active
TIGER Spine System	77675-30	FDA UDI	Class II	Active
TIGER Spine OCT System	R3512-045	FDA UDI	Class II	Active
TIGER Spine System	55675-110	FDA UDI	Class II	Active
TIGER Spine System	77865-55	FDA UDI	Class II	Active
FOUNDATION System	830845-13	FDA UDI	Class II	Active
CoreLink Foundation 3D Lateral Cage	3LL1855-0814	FDA UDI	Class II	Active
TIGER Spine System	61085-70	FDA UDI	Class II	Active
TIGER Spine System	55065-40	FDA UDI	Class II	Active
TIGER Spine System	61185-25	FDA UDI	Class II	Active
TIGER Spine System	61215-01	FDA UDI	Class II	Active
TIGER Spine OCT System	35635-20	FDA UDI	Class II	Active
CoreLink Foundation 3D Lateral Cage	3LL2250-1214	FDA UDI	Class II	Active
TIGER Spine System	60075-55	FDA UDI	Class II	Active
CoreLink Foundation 3D ALIF Stand-Alone Cage	3AS2740-2519	FDA UDI	Class II	Active
TIGER Spine System	77595-60	FDA UDI	Class II	Active
TIGER Spine System	77865-25	FDA UDI	Class II	Active
TIGER Spine System	55375-110	FDA UDI	Class II	Active
FOUNDATION System	841255-11	FDA UDI	Class II	Active
TIGER Spine System	77685-110	FDA UDI	Class II	Active
FOUNDATION System	860045-14	FDA UDI	Class II	Active
TIGER Spine System	55405-40	FDA UDI	Class II	Active

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Authorised Representatives

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Authorities

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FDA Recalls (1)

Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.

CoreLink LLC has one FDA recall record initiated on 2022-10-20, which is marked as terminated. The recall pertains to specific lots of FLXfit implants, where the manufacturer identified that internal components may have been manufactured using stainless steel instead of the stated titanium alloy.

AI-generated summary of the recall records listed below. It describes what the records state and is not an assessment of this manufacturer.

Date	Recall No.	Class	Status	Reason
Oct 20, 2022	Z-0954-2023	—	terminated	Specific lots of FLXfit implants have internal components that may have been manufactured using stainless steel rather than the specified titanium alloy.