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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 65 of 72

Device	Model / Reference	Registries	Class	Status
TIGER Spine OCT System	35935-28	FDA UDI	Class II	Active
TIGER Spine System	77575-100	FDA UDI	Class II	Active
TIGER Spine OCT System	35945-24	FDA UDI	Class II	Active
TIGER Spine System	55575-40	FDA UDI	Class II	Active
TIGER Spine OCT System	35945-40	FDA UDI	Class II	Active
CoreLink LATERAL PLATE - 2 SCREW	900215-18	FDA UDI	Class II	Unknown
TIGER Spine System	77505-110	FDA UDI	Class II	Active
TIGER Spine System	R5512-045	FDA UDI	Class II	Active
TIGER Spine System	77855-60	FDA UDI	Class II	Active
TIGER Spine System	77595-120	FDA UDI	Class II	Active
FOUNDATION System	PMW2615	FDA UDI	Class II	Active
TIGER Spine OCT System	R3556-600	FDA UDI	Class II	Active
TIGER Spine System	R5511-080	FDA UDI	Class II	Active
TIGER Spine System	R5512-150	FDA UDI	Class II	Active
TIGER Spine System	R5508-055	FDA UDI	Class II	Active
TIGER Spine System	55255-50	FDA UDI	Class II	Active
FOUNDATION System	PLW3017	FDA UDI	Class II	Active
FOUNDATION System	PM2609	FDA UDI	Class II	Active
TIGER Spine System	55080-45	FDA UDI	Class II	Active
TIGER Spine OCT System	35035-50	FDA UDI	Class II	Active
FOUNDATION System	PL3018	FDA UDI	Class II	Active
TIGER Spine System	60165-50	FDA UDI	Class II	Active
TIGER Spine System	61200-02	FDA UDI	Class II	Active
CoreLink Foundation 3D ALIF Stand-Alone Cage	3AS2540-2019	FDA UDI	Class II	Active
FOUNDATION System	TL3013	FDA UDI	Class II	Active
TIGER Spine System	R55080-40	FDA UDI	Class II	Active
FOUNDATION System	870030-07	FDA UDI	Class II	Active
TIGER Spine System	55095-55	FDA UDI	Class II	Active
FOUNDATION System	830850-14	FDA UDI	Class II	Active
FOUNDATION System	870060-08	FDA UDI	Class II	Active
TIGER Spine System	61185-80	FDA UDI	Class II	Active
FOUNDATION System	840855-15	FDA UDI	Class II	Active
CoreLink 3D Lateral Cage	3LL1850-2514	FDA UDI	Class II	Active
TIGER Spine System	77555-40	FDA UDI	Class II	Active
TIGER Spine System	77855-30	FDA UDI	Class II	Active
TIGER Spine System	55555-25	FDA UDI	Class II	Active
CoreLink Foundation 3D ALIF Stand-Alone Cage	3AS2735-2521	FDA UDI	Class II	Active
TIGER Spine System	60085-60	FDA UDI	Class II	Active
TIGER Spine System	R5514-095	FDA UDI	Class II	Active
ANODYNE Plate System	21352-18	FDA UDI	Class II	Active
CoreLink Foundation 3D ALIF Stand-Alone Cage	3AS3040-3018	FDA UDI	Class II	Active
FOUNDATION System	840045-12	FDA UDI	Class II	Active
CoreLink Foundation 3D ALIF Stand-Alone Cage	3AS2735-2020	FDA UDI	Class II	Active
TIGER Spine System	77665-50	FDA UDI	Class II	Active
FOUNDATION System	SAT1319	FDA UDI	Class II	Active
CoreLink 3D Lateral Cage	3LL1835-0012	FDA UDI	Class II	Active
ANODYNE Plate System	20003-062	FDA UDI	Class II	Active
TIGER Spine System	55375-55	FDA UDI	Class II	Active
FOUNDATION System	830855-08	FDA UDI	Class II	Active
FOUNDATION System	LAT1318	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.