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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 13 of 72

Device	Model / Reference	Registries	Class	Status
FOUNDATION System	830850-11	FDA UDI	Class II	Active
TIGER Spine OCT System	35935-36	FDA UDI	Class II	Active
TIGER Spine System	R5511-090	FDA UDI	Class II	Active
TIGER Spine System	77585-40	FDA UDI	Class II	Active
FOUNDATION System	MA1315	FDA UDI	Class II	Active
FOUNDATION System	LCL0411	FDA UDI	Class II	Active
FOUNDATION System	MA1312	FDA UDI	Class II	Active
FOUNDATION System	840055-14	FDA UDI	Class II	Active
FOUNDATION System	860060-13	FDA UDI	Class II	Active
TIGER Spine System	60065-40	FDA UDI	Class II	Active
TIGER Spine OCT System	35140-08	FDA UDI	Class II	Active
CoreLink Foundation 3D Lateral Cage	3LL1850-0814	FDA UDI	Class II	Active
ANODYNE Plate System	20004-080	FDA UDI	Class II	Active
CoreLink Foundation 3D ALIF Stand-Alone Cage	3AS2540-3019	FDA UDI	Class II	Active
CoreLink Foundation 3D Stand Alone Cage	3AS2535-1512	FDA UDI	Class II	Active
CoreLink Foundation 3D Lateral Cage	3LL1855-1212	FDA UDI	Class II	Active
TIGER Spine System	77865-40	FDA UDI	Class II	Active
TIGER Spine System	60155-55	FDA UDI	Class II	Active
TIGER Spine System	R5514-120	FDA UDI	Class II	Active
FOUNDATION System	870025-12	FDA UDI	Class II	Active
FOUNDATION System	870060-10	FDA UDI	Class II	Active
TIGER Spine System	55695-55	FDA UDI	Class II	Active
TIGER Spine System	55355-60	FDA UDI	Class II	Active
ANODYNE Plate System	20340-14	FDA UDI	Class II	Active
FOUNDATION System	860030-14	FDA UDI	Class II	Active
TIGER Spine System	55045-30	FDA UDI	Class II	Active
FOUNDATION System	MAT0719	FDA UDI	Class II	Active
TIGER Spine System	55505-110	FDA UDI	Class II	Active
ANODYNE Plate System	21002-032	FDA UDI	Class II	Active
FOUNDATION System	860040-13	FDA UDI	Class II	Active
TIGER Spine System	R55000-50	FDA UDI	Class II	Active
TIGER Spine OCT System	R3530-075	FDA UDI	Class II	Active
TIGER Spine System	R5511-450	FDA UDI	Class II	Active
TIGER Spine System	55875-35	FDA UDI	Class II	Active
TIGER Spine System	77365-30	FDA UDI	Class II	Active
TIGER Spine System	60075-40	FDA UDI	Class II	Active
TIGER Spine System	55285-110	FDA UDI	Class II	Active
TIGER Spine System	55045-50	FDA UDI	Class II	Active
TIGER Spine System	77865-45	FDA UDI	Class II	Active
CoreLink 3D Lateral Cage	3LL1845-2512	FDA UDI	Class II	Active
FOUNDATION System	LAT1316	FDA UDI	Class II	Active
TIGER Spine OCT System	35045-44	FDA UDI	Class II	Active
TIGER Spine System	55175-70	FDA UDI	Class II	Active
TIGER Spine OCT System	35835-22	FDA UDI	Class II	Active
TIGER Spine System	55605-70	FDA UDI	Class II	Active
CoreLink Foundation 3D ALIF Stand-Alone Cage	3AS2735-1513	FDA UDI	Class II	Active
TIGER Spine System	55675-120	FDA UDI	Class II	Active
FOUNDATION System	830855-15	FDA UDI	Class II	Active
CoreLink Foundation 3D ALIF Stand-Alone Cage	3AS2740-2019	FDA UDI	Class II	Active
TIGER Spine System	60155-55	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.