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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 60 of 72

Device	Model / Reference	Registries	Class	Status
TIGER Spine OCT System	35035-32	FDA UDI	Class II	Active
CoreLink Foundation 3D Lateral Cage	3LL1860-0808	FDA UDI	Class II	Active
TIGER Spine System	77675-50	FDA UDI	Class II	Active
FOUNDATION System	860060-10	FDA UDI	Class II	Active
TIGER Spine System	55605-40	FDA UDI	Class II	Active
TIGER Spine System	55595-90	FDA UDI	Class II	Active
TIGER Spine System	60165-45	FDA UDI	Class II	Active
ANODYNE Plate System	21346-16	FDA UDI	Class II	Active
TIGER Spine System	R5507-300	FDA UDI	Class II	Active
ANODYNE Plate System	20345-19	FDA UDI	Class II	Active
TIGER Spine System	R5514-080	FDA UDI	Class II	Active
FOUNDATION System	831250-10	FDA UDI	Class II	Active
TIGER Spine System	61075-120	FDA UDI	Class II	Active
TIGER Spine OCT System	35140-10	FDA UDI	Class II	Active
TIGER Spine System	55285-80	FDA UDI	Class II	Active
TIGER Spine System	R5500-050	FDA UDI	Class II	Active
TIGER Spine OCT System	R3513-120	FDA UDI	Class II	Active
TIGER Spine OCT System	R3503-060	FDA UDI	Class II	Active
TIGER Spine System	R5502-140	FDA UDI	Class II	Active
FOUNDATION System	LAT1312	FDA UDI	Class II	Active
TIGER Spine System	55505-55	FDA UDI	Class II	Active
TIGER Spine System	60175-45	FDA UDI	Class II	Active
TIGER Spine System	R5502-120	FDA UDI	Class II	Active
TIGER Spine System	61225-01	FDA UDI	Class II	Active
TIGER Spine System	55505-60	FDA UDI	Class II	Active
ANODYNE Plate System	20003-058	FDA UDI	Class II	Active
CoreLink Foundation 3D ALIF Stand-Alone Cage	3AS2535-1517	FDA UDI	Class II	Active
TIGER Spine System	61205-00	FDA UDI	Class II	Active
TIGER Spine System	77365-50	FDA UDI	Class II	Active
FOUNDATION System	860055-07	FDA UDI	Class II	Active
FOUNDATION System	840055-09	FDA UDI	Class II	Active
TIGER Spine System	77655-25	FDA UDI	Class II	Active
TIGER Spine System	55265-25	FDA UDI	Class II	Active
TIGER Spine System	77545-30	FDA UDI	Class II	Active
FOUNDATION System	MAT0715	FDA UDI	Class II	Active
TIGER Spine System	77375-60	FDA UDI	Class II	Active
TIGER Spine System	61065-40	FDA UDI	Class II	Active
TIGER Spine OCT System	R3530-100	FDA UDI	Class II	Active
TIGER Spine System	55485-110	FDA UDI	Class II	Active
FOUNDATION System	CP0010	FDA UDI	Class II	Active
TIGER Spine System	R55060-80	FDA UDI	Class II	Active
TIGER Spine System	R55070-150	FDA UDI	Class II	Active
TIGER Spine System	77605-60	FDA UDI	Class II	Active
TIGER Spine System	R5511-075	FDA UDI	Class II	Active
TIGER Spine System	55295-80	FDA UDI	Class II	Active
TIGER Spine System	R5504-045	FDA UDI	Class II	Active
TIGER Spine OCT System	R3502-095	FDA UDI	Class II	Active
TIGER Spine System	R5514-140	FDA UDI	Class II	Active
TIGER Spine System	R55060-40	FDA UDI	Class II	Active
FOUNDATION System	830045-10	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.