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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 7 of 72

Device	Model / Reference	Registries	Class	Status
TIGER Spine System	55205-120	FDA UDI	Class II	Active
TIGER Spine System	60185-30	FDA UDI	Class II	Active
TIGER Spine System	61075-120	FDA UDI	Class II	Active
TIGER Spine OCT System	R3501-065	FDA UDI	Class II	Active
TIGER Spine System	61085-100	FDA UDI	Class II	Active
FOUNDATION System	XAT0711	FDA UDI	Class II	Active
TIGER Spine System	55455-25	FDA UDI	Class II	Active
FOUNDATION System	841255-15	FDA UDI	Class II	Active
TIGER Spine System	55685-70	FDA UDI	Class II	Active
TIGER Spine System	55855-50	FDA UDI	Class II	Active
TIGER Spine System	55185-60	FDA UDI	Class II	Active
ANODYNE Plate System	20001-011	FDA UDI	Class II	Active
TIGER Spine System	60155-50	FDA UDI	Class II	Active
TIGER Spine System	55205-70	FDA UDI	Class II	Active
TIGER Spine System	77875-50	FDA UDI	Class II	Active
TIGER Spine System	55255-45	FDA UDI	Class II	Active
TIGER Spine System	77585-45	FDA UDI	Class II	Active
CoreLink Foundation 3D ALIF Stand-Alone Cage	3AS3045-3020	FDA UDI	Class II	Active
TIGER Spine System	55595-35	FDA UDI	Class II	Active
FOUNDATION System	LA0720	FDA UDI	Class II	Active
TIGER Spine System	60175-50	FDA UDI	Class II	Active
TIGER Spine System	55675-35	FDA UDI	Class II	Active
ANODYNE Plate System	20002-036	FDA UDI	Class II	Active
CoreLink 3D Lateral Cage	3LL1850-3018	FDA UDI	Class II	Active
TIGER Spine System	55255-35	FDA UDI	Class II	Active
TIGER Spine System	R5510-060	FDA UDI	Class II	Active
TIGER Spine System	R55090-110	FDA UDI	Class II	Active
CoreLink Foundation 3D ALIF Stand-Alone Cage	3AS2740-0818	FDA UDI	Class II	Active
FOUNDATION System	870045-09	FDA UDI	Class II	Active
TIGER Spine System	77595-40	FDA UDI	Class II	Active
FOUNDATION System	LA1317	FDA UDI	Class II	Active
TIGER Spine System	5500-11	FDA UDI	Class II	Active
TIGER Spine System	77585-35	FDA UDI	Class II	Active
TIGER Spine System	60055-50	FDA UDI	Class II	Active
FOUNDATION System	LA1315	FDA UDI	Class II	Active
FOUNDATION System	860025-14	FDA UDI	Class II	Active
FOUNDATION System	PLW3214	FDA UDI	Class II	Active
TIGER Spine System	55495-35	FDA UDI	Class II	Active
TIGER Spine System	55665-45	FDA UDI	Class II	Active
TIGER Spine OCT System	35302-16	FDA UDI	Class II	Active
ANODYNE Plate System	20445-17	FDA UDI	Class II	Active
CoreLink Foundation 3D Lateral Cage	3LL2245-0008	FDA UDI	Class II	Active
TIGER Spine System	R5512-065	FDA UDI	Class II	Active
TIGER Spine System	TC5500-14	FDA UDI	Class II	Active
TIGER Spine System	55075-60	FDA UDI	Class II	Active
TIGER Spine OCT System	R3530-085	FDA UDI	Class II	Active
FOUNDATION System	830860-13	FDA UDI	Class II	Active
FOUNDATION System	LA0719	FDA UDI	Class II	Active
FOUNDATION System	870045-15	FDA UDI	Class II	Active
TIGER Spine System	R5513-500	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.