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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 62 of 72

Device	Model / Reference	Registries	Class	Status
FOUNDATION System	TM2513	FDA UDI	Class II	Active
TIGER Spine OCT System	R3502-040	FDA UDI	Class II	Active
FOUNDATION System	XAT1311	FDA UDI	Class II	Active
FOUNDATION System	830855-13	FDA UDI	Class II	Active
TIGER Spine System	61215-00	FDA UDI	Class II	Active
TIGER Spine System	55875-120	FDA UDI	Class II	Active
FOUNDATION System	840045-11	FDA UDI	Class II	Active
ANODYNE Plate System	21452-16	FDA UDI	Class II	Active
TIGER Spine System	60175-40	FDA UDI	Class II	Active
CoreLink 3D Lateral Cage	3LL2255-2514	FDA UDI	Class II	Active
CoreLink Foundation 3D ALIF Stand-Alone Cage	3AS3040-1514	FDA UDI	Class II	Active
TIGER Spine OCT System	R3531-135	FDA UDI	Class II	Active
FOUNDATION System	830050-09	FDA UDI	Class II	Active
TIGER Spine System	61155-50	FDA UDI	Class II	Active
FOUNDATION System	MA1309	FDA UDI	Class II	Active
FOUNDATION System	SAT1314	FDA UDI	Class II	Active
TIGER Spine System	55045-55	FDA UDI	Class II	Active
TIGER Spine System	R5501-300	FDA UDI	Class II	Active
CoreLink Foundation 3D ALIF Stand-Alone Cage	3AS2740-2515	FDA UDI	Class II	Active
FOUNDATION System	MA1317	FDA UDI	Class II	Active
TIGER Spine System	55005-60	FDA UDI	Class II	Active
CoreLink Foundation 3D ALIF Stand-Alone Cage	3AS2540-0819	FDA UDI	Class II	Active
CoreLink 3D Lateral Cage	3LL1855-3020	FDA UDI	Class II	Active
FOUNDATION System	830040-10	FDA UDI	Class II	Active
TIGER Spine System	R5503-300	FDA UDI	Class II	Active
FOUNDATION System	830850-09	FDA UDI	Class II	Active
TIGER Spine System	55595-100	FDA UDI	Class II	Active
FOUNDATION System	XCL0712	FDA UDI	Class II	Active
TIGER Spine System	55405-60	FDA UDI	Class II	Active
ANODYNE Plate System	20003-048	FDA UDI	Class II	Active
CoreLink 3D Lateral Cage	3LL1855-2518	FDA UDI	Class II	Active
TIGER Spine System	61075-35	FDA UDI	Class II	Active
FOUNDATION System	840850-14	FDA UDI	Class II	Active
CoreLink 3D Lateral Cage	3LL2260-0014	FDA UDI	Class II	Active
TIGER Spine System	77865-40	FDA UDI	Class II	Active
TIGER Spine System	61185-100	FDA UDI	Class II	Active
CoreLink Foundation 3D Lateral Cage	3LL1845-0814	FDA UDI	Class II	Active
TIGER Spine System	61065-80	FDA UDI	Class II	Active
TIGER Spine System	55695-40	FDA UDI	Class II	Active
FOUNDATION System	860025-08	FDA UDI	Class II	Active
TIGER Spine System	55565-30	FDA UDI	Class II	Active
TIGER Spine System	61200-01	FDA UDI	Class II	Active
TIGER Spine System	77865-35	FDA UDI	Class II	Active
TIGER Spine System	77585-90	FDA UDI	Class II	Active
TIGER Spine System	R5506-045	FDA UDI	Class II	Active
TIGER Spine System	77565-45	FDA UDI	Class II	Active
TIGER Spine System	61165-80	FDA UDI	Class II	Active
CoreLink Foundation 3D ALIF Stand-Alone Cage	3AS3045-1519	FDA UDI	Class II	Active
FOUNDATION System	870040-14	FDA UDI	Class II	Active
TIGER Spine System	55070-60	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.