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CORELINK LLC

Last updated May 24, 2026

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 66 of 72

Device	Model / Reference	Registries	Class	Status
TIGER Spine System	55331-200	FDA UDI	Class II	Active
TIGER Spine System	55075-55	FDA UDI	Class II	Active
FOUNDATION System	860030-06	FDA UDI	Class II	Active
ANODYNE Plate System	20445-15	FDA UDI	Class II	Active
ANODYNE Plate System	20002-028	FDA UDI	Class II	Active
TIGER Spine System	77695-90	FDA UDI	Class II	Active
TIGER Spine System	60175-55	FDA UDI	Class II	Active
TIGER Spine OCT System	35040-10	FDA UDI	Class II	Active
FOUNDATION System	860030-16	FDA UDI	Class II	Active
CoreLink LATERAL SCREW	90755-35	FDA UDI	Class II	Active
TIGER Spine System	55001-3	FDA UDI	Class II	Active
TIGER Spine System	R5500-045	FDA UDI	Class II	Active
TIGER Spine OCT System	R3530-125	FDA UDI	Class II	Active
TIGER Spine System	77555-30	FDA UDI	Class II	Active
CoreLink Foundation 3D ALIF Stand-Alone Cage	3AS2540-0810	FDA UDI	Class II	Active
TIGER Spine System	77375-50	FDA UDI	Class II	Active
CoreLink LATERAL SCREW	90755-55	FDA UDI	Class II	Active
CoreLink 3D Lateral Cage	3LL1835-0008	FDA UDI	Class II	Active
TIGER Spine System	R5504-055	FDA UDI	Class II	Active
TIGER Spine System	60215-01	FDA UDI	Class II	Active
TIGER Spine System	77585-100	FDA UDI	Class II	Active
TIGER Spine OCT System	35945-36	FDA UDI	Class II	Active
TIGER Spine System	R5508-060	FDA UDI	Class II	Active
ANODYNE Plate System	20145-18	FDA UDI	Class II	Active
TIGER Spine System	55845-55	FDA UDI	Class II	Active
TIGER Spine System	77595-40	FDA UDI	Class II	Active
TIGER Spine System	60175-60	FDA UDI	Class II	Active
TIGER Spine System	R5505-060	FDA UDI	Class II	Active
TIGER Spine System	77505-35	FDA UDI	Class II	Active
TIGER Spine System	55865-50	FDA UDI	Class II	Active
CoreLink 3D Lateral Cage	3LL1845-2014	FDA UDI	Class II	Active
TIGER Spine System	61155-25	FDA UDI	Class II	Active
ANODYNE Plate System	21346-12	FDA UDI	Class II	Active
FOUNDATION System	PLW3012	FDA UDI	Class II	Active
ANODYNE Plate System	21352-12	FDA UDI	Class II	Active
TIGER Spine System	55865-40	FDA UDI	Class II	Active
TIGER Spine System	55195-60	FDA UDI	Class II	Active
ANODYNE Plate System	21146-20	FDA UDI	Class II	Active
TIGER Spine System	55455-45	FDA UDI	Class II	Active
TIGER Spine System	55695-100	FDA UDI	Class II	Active
TIGER Spine OCT System	35845-32	FDA UDI	Class II	Active
TIGER Spine System	55845-25	FDA UDI	Class II	Active
TIGER Spine OCT System	35845-34	FDA UDI	Class II	Active
TIGER Spine System	55245-55	FDA UDI	Class II	Active
CoreLink Foundation 3D Lateral Cage	3LL2260-3018	FDA UDI	Class II	Active
CoreLink Foundation 3D ALIF Stand-Alone Cage	3AS2735-1512	FDA UDI	Class II	Active
TIGER Spine System	R5510-080	FDA UDI	Class II	Active
FOUNDATION System	SA0714	FDA UDI	Class II	Active
TIGER Spine System	60225-01	FDA UDI	Class II	Active
TIGER Spine System	55000-51	FDA UDI	Class II	Active

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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.

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.