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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 9 of 72

Device	Model / Reference	Registries	Class	Status
TIGER Spine System	77875-100	FDA UDI	Class II	Active
TIGER Spine System	77695-70	FDA UDI	Class II	Active
CoreLink Foundation 3D ALIF Stand-Alone Cage	3AS3040-0817	FDA UDI	Class II	Active
CoreLink Foundation 3D ALIF Stand-Alone Cage	3AS2740-2018	FDA UDI	Class II	Active
TIGER Spine System	77585-40	FDA UDI	Class II	Active
TIGER Spine System	R55080-50	FDA UDI	Class II	Active
CoreLink 3D Lateral Cage	3LL2245-2516	FDA UDI	Class II	Active
TIGER Spine System	61065-25	FDA UDI	Class II	Active
TIGER Spine OCT System	35945-26	FDA UDI	Class II	Active
TIGER Spine System	77605-55	FDA UDI	Class II	Active
TIGER Spine System	77655-40	FDA UDI	Class II	Active
TIGER Spine System	R55060-120	FDA UDI	Class II	Active
TIGER Spine System	55095-110	FDA UDI	Class II	Active
TIGER Spine OCT System	35045-40	FDA UDI	Class II	Active
CoreLink Foundation 3D Lateral Cage	3LL2260-0808	FDA UDI	Class II	Active
TIGER Spine System	60185-45	FDA UDI	Class II	Active
TIGER Spine System	R5502-060	FDA UDI	Class II	Active
TIGER Spine System	55065-35	FDA UDI	Class II	Active
TIGER Spine System	60065-30	FDA UDI	Class II	Active
TIGER Spine System	55295-100	FDA UDI	Class II	Active
FOUNDATION System	TL3015	FDA UDI	Class II	Active
TIGER Spine OCT System	35150-06	FDA UDI	Class II	Active
CoreLink Foundation 3D ALIF Stand-Alone Cage	3AS2540-0814	FDA UDI	Class II	Active
FOUNDATION System	870035-07	FDA UDI	Class II	Active
TIGER Spine System	55065-45	FDA UDI	Class II	Active
TIGER Spine System	60075-25	FDA UDI	Class II	Active
FOUNDATION System	PLW3212	FDA UDI	Class II	Active
TIGER Spine System	R5510-100	FDA UDI	Class II	Active
TIGER Spine System	R55080-90	FDA UDI	Class II	Active
CoreLink Foundation 3D ALIF Stand-Alone Cage	3AS2735-2520	FDA UDI	Class II	Active
TIGER Spine System	60065-35	FDA UDI	Class II	Active
FOUNDATION System	870060-12	FDA UDI	Class II	Active
FOUNDATION System	PS2210	FDA UDI	Class II	Active
CoreLink Foundation 3D ALIF Stand Alone Cage	3AS2535-0810	FDA UDI	Class II	Active
TIGER Spine System	77575-60	FDA UDI	Class II	Active
TIGER Spine System	55865-60	FDA UDI	Class II	Active
TIGER Spine System	55001-10	FDA UDI	Class II	Active
TIGER Spine OCT System	R3531-095	FDA UDI	Class II	Active
CoreLink 3D Lateral Cage	3LL1850-0012	FDA UDI	Class II	Active
TIGER Spine System	55575-35	FDA UDI	Class II	Active
FOUNDATION System	870035-09	FDA UDI	Class II	Active
TIGER Spine System	77865-45	FDA UDI	Class II	Active
CoreLink 3D Lateral Cage	3LL1840-0010	FDA UDI	Class II	Active
TIGER Spine System	77875-80	FDA UDI	Class II	Active
TIGER Spine System	60200-02	FDA UDI	Class II	Active
TIGER Spine System	R55090-150	FDA UDI	Class II	Active
TIGER Spine System	R5512-100	FDA UDI	Class II	Active
TIGER Spine System	77675-70	FDA UDI	Class II	Active
TIGER Spine System	60165-55	FDA UDI	Class II	Active
TIGER Spine System	77375-90	FDA UDI	Class II	Active

Related Companies

Authorised Representatives

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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.