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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 68 of 72

Device	Model / Reference	Registries	Class	Status
TIGER Spine System	55565-40	FDA UDI	Class II	Active
FOUNDATION System	LAT1309	FDA UDI	Class II	Active
TIGER Spine System	55605-55	FDA UDI	Class II	Active
CoreLink 3D Lateral Cage	3LL2240-0012	FDA UDI	Class II	Active
CoreLink Foundation 3D ALIF Stand-Alone Cage	3AS3040-2020	FDA UDI	Class II	Active
TIGER Spine System	R5510-150	FDA UDI	Class II	Active
TIGER Spine System	R55000-150	FDA UDI	Class II	Active
TIGER Spine System	77685-55	FDA UDI	Class II	Active
TIGER Spine System	R5509-080	FDA UDI	Class II	Active
TIGER Spine System	55050-45	FDA UDI	Class II	Active
CoreLink Foundation 3D ALIF Stand-Alone Cage	3AS2540-2519	FDA UDI	Class II	Active
TIGER Spine System	77675-50	FDA UDI	Class II	Active
TIGER Spine OCT System	35035-38	FDA UDI	Class II	Active
CoreLink Foundation 3D ALIF Stand-Alone Cage	3AS3045-2518	FDA UDI	Class II	Active
TIGER Spine System	61075-50	FDA UDI	Class II	Active
TIGER Spine System	61175-70	FDA UDI	Class II	Active
TIGER Spine System	77685-40	FDA UDI	Class II	Active
FOUNDATION System	LA1316	FDA UDI	Class II	Active
TIGER Spine System	61075-90	FDA UDI	Class II	Active
TIGER Spine OCT System	35255-50	FDA UDI	Class II	Active
TIGER Spine System	55345-35	FDA UDI	Class II	Active
TIGER Spine System	R55090-55	FDA UDI	Class II	Active
CoreLink 3D Lateral Cage	3LL1855-2018	FDA UDI	Class II	Active
TIGER Spine System	60155-25	FDA UDI	Class II	Active
FOUNDATION System	LCL0410	FDA UDI	Class II	Active
TIGER Spine System	77575-35	FDA UDI	Class II	Active
CoreLink Foundation 3D ALIF Stand-Alone Cage	3AS3045-0813	FDA UDI	Class II	Active
FOUNDATION System	840050-09	FDA UDI	Class II	Active
TIGER Spine System	60155-45	FDA UDI	Class II	Active
TIGER Spine System	R55060-60	FDA UDI	Class II	Active
TIGER Spine System	55855-40	FDA UDI	Class II	Active
FOUNDATION System	TM2507	FDA UDI	Class II	Active
TIGER Spine System	60055-30	FDA UDI	Class II	Active
ANODYNE Plate System	20245-16	FDA UDI	Class II	Active
FOUNDATION System	MAT1318	FDA UDI	Class II	Active
FOUNDATION System	MAT0713	FDA UDI	Class II	Active
TIGER Spine OCT System	35835-10	FDA UDI	Class II	Active
ZOU Plate System	10000-017	FDA UDI	Class II	Active
FOUNDATION System	840840-09	FDA UDI	Class II	Active
TIGER Spine OCT System	R3510-035	FDA UDI	Class II	Active
CoreLink Foundation 3D ALIF Stand-Alone Cage	3AS3040-2516	FDA UDI	Class II	Active
TIGER Spine System	60065-35	FDA UDI	Class II	Active
FOUNDATION System	830060-08	FDA UDI	Class II	Active
TIGER Spine System	77585-110	FDA UDI	Class II	Active
TIGER Spine System	60185-30	FDA UDI	Class II	Active
FOUNDATION System	860040-08	FDA UDI	Class II	Active
TIGER Spine System	55875-60	FDA UDI	Class II	Active
CoreLink Foundation 3D ALIF Stand-Alone Cage	3AS3040-0812	FDA UDI	Class II	Active
TIGER Spine OCT System	R3503-055	FDA UDI	Class II	Active
FOUNDATION System	841250-11	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.