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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 59 of 72

Device	Model / Reference	Registries	Class	Status
TIGER Spine System	R55090-70	FDA UDI	Class II	Active
FOUNDATION System	841250-16	FDA UDI	Class II	Active
TIGER Spine System	61085-70	FDA UDI	Class II	Active
TIGER Spine System	77575-45	FDA UDI	Class II	Active
TIGER Spine System	60185-25	FDA UDI	Class II	Active
TIGER Spine System	55255-25	FDA UDI	Class II	Active
TIGER Spine System	55000-20	FDA UDI	Class II	Active
TIGER Spine System	77545-50	FDA UDI	Class II	Active
CoreLink Foundation 3D ALIF Stand-Alone Cage	3AS2540-2015	FDA UDI	Class II	Active
TIGER Spine System	77355-35	FDA UDI	Class II	Active
TIGER Spine System	55675-70	FDA UDI	Class II	Active
CoreLink Foundation 3D ALIF Stand-Alone Cage	3AS3045-3021	FDA UDI	Class II	Active
FOUNDATION System	880030-15	FDA UDI	Class II	Active
CoreLink Foundation 3D Lateral Cage	3LL1860-0814	FDA UDI	Class II	Active
TIGER Spine System	51075-30	FDA UDI	Class II	Active
FOUNDATION System	MA0710	FDA UDI	Class II	Active
FOUNDATION System	860035-06	FDA UDI	Class II	Active
TIGER Spine System	61165-55	FDA UDI	Class II	Active
FOUNDATION System	870030-08	FDA UDI	Class II	Active
ANODYNE Plate System	21002-038	FDA UDI	Class II	Active
TIGER Spine System	77605-90	FDA UDI	Class II	Active
TIGER Spine System	61185-35	FDA UDI	Class II	Active
CoreLink 3D Lateral Cage	3LL2235-0008	FDA UDI	Class II	Active
CoreLink Foundation 3D ALIF Stand-Alone Cage	3AS2735-3021	FDA UDI	Class II	Active
TIGER Spine System	55245-40	FDA UDI	Class II	Active
TIGER Spine System	55595-120	FDA UDI	Class II	Active
TIGER Spine OCT System	R3500-070	FDA UDI	Class II	Active
TIGER Spine System	61200-00	FDA UDI	Class II	Active
TIGER Spine System	77675-70	FDA UDI	Class II	Active
TIGER Spine OCT System	R3511-040	FDA UDI	Class II	Active
TIGER Spine System	55045-30	FDA UDI	Class II	Active
FOUNDATION System	860045-13	FDA UDI	Class II	Active
TIGER Spine System	61085-55	FDA UDI	Class II	Active
CoreLink Foundation 3D ALIF Stand-Alone Cage	3AS2540-1512	FDA UDI	Class II	Active
CoreLink Foundation 3D ALIF Stand-Alone Cage	3AS3045-1511	FDA UDI	Class II	Active
FOUNDATION System	830845-11	FDA UDI	Class II	Active
FOUNDATION System	PMW2617	FDA UDI	Class II	Active
TIGER Spine System	R5507-050	FDA UDI	Class II	Active
FOUNDATION System	PL3013	FDA UDI	Class II	Active
TIGER Spine System	61175-70	FDA UDI	Class II	Active
TIGER Spine System	61065-35	FDA UDI	Class II	Active
TIGER Spine System	55070-40	FDA UDI	Class II	Active
TIGER Spine System	77585-55	FDA UDI	Class II	Active
TIGER Spine System	51065-60	FDA UDI	Class II	Active
TIGER Spine System	77575-55	FDA UDI	Class II	Active
TIGER Spine System	R5506-075	FDA UDI	Class II	Active
FOUNDATION System	840045-09	FDA UDI	Class II	Active
FOUNDATION System	840055-13	FDA UDI	Class II	Active
TIGER Spine System	60185-60	FDA UDI	Class II	Active
CoreLink Foundation 3D ALIF Stand-Alone Cage	3AS3045-2018	FDA UDI	Class II	Active

Related Companies

Authorised Representatives

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Importers

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Notified Bodies

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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.