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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 2 of 72

Device	Model / Reference	Registries	Class	Status
CoreLink 3D Lateral Cage	3LL1840-0808	FDA UDI	Class II	Active
TIGER Spine System	R5500-075	FDA UDI	Class II	Active
TIGER Spine System	55875-30	FDA UDI	Class II	Active
TIGER Spine System	60325-20	FDA UDI	Class II	Active
TIGER Spine System	55275-35	FDA UDI	Class II	Active
CoreLink Foundation 3D Lateral Cage	3LL2260-0814	FDA UDI	Class II	Active
FOUNDATION System	TM2512	FDA UDI	Class II	Active
TIGER Spine System	55355-40	FDA UDI	Class II	Active
FOUNDATION System	840855-10	FDA UDI	Class II	Active
TIGER Spine System	77575-80	FDA UDI	Class II	Active
FOUNDATION System	870035-13	FDA UDI	Class II	Active
FOUNDATION System	PL3016	FDA UDI	Class II	Active
TIGER Spine System	61185-50	FDA UDI	Class II	Active
ANODYNE Plate System	20003-070	FDA UDI	Class II	Active
TIGER Spine System	61155-40	FDA UDI	Class II	Active
FOUNDATION System	860035-14	FDA UDI	Class II	Active
TIGER Spine OCT System	35150-16	FDA UDI	Class II	Active
FOUNDATION System	LA1320	FDA UDI	Class II	Active
TIGER Spine System	R5514-130	FDA UDI	Class II	Active
TIGER Spine OCT System	35945-22	FDA UDI	Class II	Active
TIGER Spine System	55085-55	FDA UDI	Class II	Active
TIGER Spine System	77355-45	FDA UDI	Class II	Active
TIGER Spine System	R5502-035	FDA UDI	Class II	Active
TIGER Spine System	R5502-150	FDA UDI	Class II	Active
TIGER Spine System	77505-120	FDA UDI	Class II	Active
FOUNDATION System	840850-12	FDA UDI	Class II	Active
FOUNDATION System	PMW2614	FDA UDI	Class II	Active
TIGER Spine System	77875-70	FDA UDI	Class II	Active
TIGER Spine System	77685-35	FDA UDI	Class II	Active
TIGER Spine System	61175-60	FDA UDI	Class II	Active
FOUNDATION System	MA0716	FDA UDI	Class II	Active
FOUNDATION System	880040-09	FDA UDI	Class II	Active
TIGER Spine System	77675-40	FDA UDI	Class II	Active
F3D Cervical Cage	3CFLLWW-LLHH	FDA UDI	Class II	Active
CoreLink 3D Lateral Cage	3LL1835-0810	FDA UDI	Class II	Active
TIGER Spine System	60085-35	FDA UDI	Class II	Active
TIGER Spine System	61205-00	FDA UDI	Class II	Active
TIGER Spine System	60330-20	FDA UDI	Class II	Active
TIGER Spine System	R55060-140	FDA UDI	Class II	Active
CoreLink 3D Lateral Cage	3LL2255-2016	FDA UDI	Class II	Active
TIGER Spine System	R5503-400	FDA UDI	Class II	Active
TIGER Spine OCT System	R3513-030	FDA UDI	Class II	Active
TIGER Spine System	77875-90	FDA UDI	Class II	Active
TIGER Spine System	55845-35	FDA UDI	Class II	Active
TIGER Spine System	55475-35	FDA UDI	Class II	Active
TIGER Spine System	R55000-80	FDA UDI	Class II	Active
FOUNDATION System	830845-16	FDA UDI	Class II	Active
TIGER Spine System	77505-50	FDA UDI	Class II	Active
FOUNDATION System	840860-08	FDA UDI	Class II	Active
TIGER Spine System	77695-80	FDA UDI	Class II	Active

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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.

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.