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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 3 of 72

Device	Model / Reference	Registries	Class	Status
TIGER Spine System	61055-35	FDA UDI	Class II	Active
CoreLink Foundation 3D ALIF Stand-Alone Cage	3AS3045-0810	FDA UDI	Class II	Active
TIGER Spine System	61075-80	FDA UDI	Class II	Active
ANODYNE Plate System	20445-20	FDA UDI	Class II	Active
ANODYNE Plate System	20003-040	FDA UDI	Class II	Active
TIGER Spine System	R5505-100	FDA UDI	Class II	Active
CoreLink LATERAL SCREW	900415-20	FDA UDI	Class II	Active
TIGER Spine System	61075-110	FDA UDI	Class II	Active
TIGER Spine System	55465-25	FDA UDI	Class II	Active
TIGER Spine System	55301-30	FDA UDI	Class II	Active
CoreLink Foundation 3D ALIF Stand-Alone Cage	3AS3040-2014	FDA UDI	Class II	Active
CoreLink 3D Lateral Cage	3LL2250-2516	FDA UDI	Class II	Active
TIGER Spine System	R55000-90	FDA UDI	Class II	Active
TIGER Spine OCT System	R3530-120	FDA UDI	Class II	Active
TIGER Spine System	60210-01	FDA UDI	Class II	Active
ANODYNE Plate System	20440-20	FDA UDI	Class II	Active
CoreLink Foundation 3D Lateral Cage	3LL2260-1214	FDA UDI	Class II	Active
CoreLink Foundation 3D ALIF Stand-Alone Cage	3AS2535-0821	FDA UDI	Class II	Active
ANODYNE Plate System	20140-12	FDA UDI	Class II	Active
FOUNDATION System	XCL0705	FDA UDI	Class II	Active
FOUNDATION System	870045-16	FDA UDI	Class II	Active
FOUNDATION System	LA1319	FDA UDI	Class II	Active
TIGER Spine System	60165-40	FDA UDI	Class II	Active
TIGER Spine System	77595-90	FDA UDI	Class II	Active
TIGER Spine System	61155-55	FDA UDI	Class II	Active
TIGER Spine System	77675-90	FDA UDI	Class II	Active
TIGER Spine System	61075-60	FDA UDI	Class II	Active
TIGER Spine OCT System	35740-20	FDA UDI	Class II	Active
FOUNDATION System	840850-11	FDA UDI	Class II	Active
CoreLink Foundation 3D ALIF Stand-Alone Cage	3AS3045-2517	FDA UDI	Class II	Active
TIGER Spine System	77695-35	FDA UDI	Class II	Active
TIGER Spine System	55075-25	FDA UDI	Class II	Active
CoreLink Foundation 3D ALIF Stand-Alone Cage	3AS2540-2515	FDA UDI	Class II	Active
TIGER Spine OCT System	35045-28	FDA UDI	Class II	Active
TIGER Spine System	77575-70	FDA UDI	Class II	Active
FOUNDATION System	830060-13	FDA UDI	Class II	Active
CoreLink Foundation 3D ALIF Stand-Alone Cage	3AS2735-0811	FDA UDI	Class II	Active
TIGER Spine System	55685-110	FDA UDI	Class II	Active
TIGER Spine System	55495-100	FDA UDI	Class II	Active
TIGER Spine System	77605-55	FDA UDI	Class II	Active
ANODYNE Plate System	21452-14	FDA UDI	Class II	Active
FOUNDATION System	XAT0718	FDA UDI	Class II	Active
ANODYNE Plate System	21002-040	FDA UDI	Class II	Active
FOUNDATION System	PLW3011	FDA UDI	Class II	Active
TIGER Spine System	60155-25	FDA UDI	Class II	Active
CoreLink Foundation 3D ALIF Stand-Alone Cage	3AS3040-3021	FDA UDI	Class II	Active
TIGER Spine OCT System	R3503-050	FDA UDI	Class II	Active
TIGER Spine System	61165-40	FDA UDI	Class II	Active
TIGER Spine System	61065-60	FDA UDI	Class II	Active
FOUNDATION System	830845-15	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.