Is this your brand? Sign in to claim ownership.

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 4 of 72

Device	Model / Reference	Registries	Class	Status
TIGER Spine System	55405-110	FDA UDI	Class II	Active
TIGER Spine System	R5511-085	FDA UDI	Class II	Active
TIGER Spine System	55675-50	FDA UDI	Class II	Active
TIGER Spine System	R5514-150	FDA UDI	Class II	Active
TIGER Spine System	55345-55	FDA UDI	Class II	Active
TIGER Spine System	77665-55	FDA UDI	Class II	Active
FOUNDATION System	831255-13	FDA UDI	Class II	Active
CoreLink Foundation 3D Lateral Cage	3LL1850-0808	FDA UDI	Class II	Active
TIGER Spine OCT System	35045-20	FDA UDI	Class II	Active
FOUNDATION System	830045-09	FDA UDI	Class II	Active
TIGER Spine System	60075-45	FDA UDI	Class II	Active
FOUNDATION System	CL0410	FDA UDI	Class II	Active
TIGER Spine System	77365-55	FDA UDI	Class II	Active
FOUNDATION System	MAT0712	FDA UDI	Class II	Active
TIGER Spine System	R5511-070	FDA UDI	Class II	Active
FOUNDATION System	830845-12	FDA UDI	Class II	Active
FOUNDATION System	LA0713	FDA UDI	Class II	Active
CoreLink Foundation 3D ALIF Stand-Alone Cage	3AS3045-1514	FDA UDI	Class II	Active
TIGER Spine System	77375-70	FDA UDI	Class II	Active
TIGER Spine System	R5506-035	FDA UDI	Class II	Active
FOUNDATION System	880030-12	FDA UDI	Class II	Active
FOUNDATION System	MA1318	FDA UDI	Class II	Active
CoreLink 3D Lateral Cage	3LL2250-2014	FDA UDI	Class II	Active
TIGER Spine System	R5507-055	FDA UDI	Class II	Active
FOUNDATION System	870045-14	FDA UDI	Class II	Active
TIGER Spine System	61175-80	FDA UDI	Class II	Active
CoreLink Foundation 3D ALIF Stand-Alone Cage	3AS2535-1515	FDA UDI	Class II	Active
TIGER Spine System	55375-100	FDA UDI	Class II	Active
TIGER Spine System	55665-50	FDA UDI	Class II	Active
TIGER Spine System	R5509-085	FDA UDI	Class II	Active
FOUNDATION System	LCP0008	FDA UDI	Class II	Active
TIGER Spine System	R55090-450	FDA UDI	Class II	Active
TIGER Spine System	77675-45	FDA UDI	Class II	Active
CoreLink Foundation 3D Lateral Cage	3LL2245-0810	FDA UDI	Class II	Active
TIGER Spine System	55685-90	FDA UDI	Class II	Active
TIGER Spine System	77875-120	FDA UDI	Class II	Active
FOUNDATION System	880040-15	FDA UDI	Class II	Active
TIGER Spine System	55175-120	FDA UDI	Class II	Active
FOUNDATION System	860025-12	FDA UDI	Class II	Active
TIGER Spine System	61085-50	FDA UDI	Class II	Active
FOUNDATION System	860030-09	FDA UDI	Class II	Active
CoreLink Foundation 3D Lateral Cage	3LL1845-0808	FDA UDI	Class II	Active
FOUNDATION System	880035-07	FDA UDI	Class II	Active
CoreLink Foundation 3D Stand Alone Screw	10365-25	FDA UDI	Class II	Active
ANODYNE Plate System	21346-20	FDA UDI	Class II	Active
TIGER Spine System	55345-60	FDA UDI	Class II	Active
TIGER Spine OCT System	R3503-070	FDA UDI	Class II	Active
TIGER Spine System	55105-70	FDA UDI	Class II	Active
TIGER Spine System	60075-35	FDA UDI	Class II	Active
TIGER Spine System	77605-45	FDA UDI	Class II	Active

Related Companies

Authorised Representatives

No authorised representatives on record.

Importers

Not available yet.

Notified Bodies

Not available yet.

Authorities

Not available yet.

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.