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 5 of 72

Device	Model / Reference	Registries	Class	Status
TIGER Spine System	55455-35	FDA UDI	Class II	Active
TIGER Spine System	55175-90	FDA UDI	Class II	Active
FOUNDATION System	SA1309	FDA UDI	Class II	Active
TIGER Spine System	55875-25	FDA UDI	Class II	Active
TIGER Spine System	55085-45	FDA UDI	Class II	Active
TIGER Spine System	55655-25	FDA UDI	Class II	Active
TIGER Spine System	60220-01	FDA UDI	Class II	Active
TIGER Spine System	55000-15	FDA UDI	Class II	Active
ANODYNE Plate System	20345-14	FDA UDI	Class II	Active
FOUNDATION System	MAT0710	FDA UDI	Class II	Active
TIGER Spine System	55355-60	FDA UDI	Class II	Active
TIGER Spine System	55065-50	FDA UDI	Class II	Active
FOUNDATION System	870040-08	FDA UDI	Class II	Active
TIGER Spine System	55095-70	FDA UDI	Class II	Active
TIGER Spine OCT System	R3501-090	FDA UDI	Class II	Active
TIGER Spine System	61155-35	FDA UDI	Class II	Active
ANODYNE Plate System	20240-19	FDA UDI	Class II	Active
TIGER Spine System	55865-55	FDA UDI	Class II	Active
TIGER Spine System	55475-60	FDA UDI	Class II	Active
CoreLink LATERAL PLATE	900115-28	FDA UDI	Class II	Active
TIGER Spine System	55245-25	FDA UDI	Class II	Active
FOUNDATION System	860030-13	FDA UDI	Class II	Active
CoreLink Foundation 3D ALIF Stand-Alone Cage	3AS3040-1510	FDA UDI	Class II	Active
TIGER Spine System	60065-50	FDA UDI	Class II	Active
TIGER Spine System	61085-40	FDA UDI	Class II	Active
TIGER Spine System	R5506-040	FDA UDI	Class II	Active
TIGER Spine OCT System	R3512-240	FDA UDI	Class II	Active
TIGER Spine System	55245-50	FDA UDI	Class II	Active
FOUNDATION System	LAT0713	FDA UDI	Class II	Active
CoreLink 3D Lateral Cage	3LL2245-2014	FDA UDI	Class II	Active
FOUNDATION System	860060-12	FDA UDI	Class II	Active
TIGER Spine System	55845-40	FDA UDI	Class II	Active
CoreLink Foundation 3D Stand Alone Screw	10355-25	FDA UDI	Class II	Active
TIGER Spine System	55565-45	FDA UDI	Class II	Active
CoreLink Foundation 3D ALIF Stand-Alone Cage	3AS2540-1510	FDA UDI	Class II	Active
TIGER Spine System	77595-120	FDA UDI	Class II	Active
CoreLink 3D Lateral Cage	3LL1845-0010	FDA UDI	Class II	Active
TIGER Spine System	R5505-120	FDA UDI	Class II	Active
CoreLink Foundation 3D ALIF Stand-Alone Cage	3AS3040-1516	FDA UDI	Class II	Active
TIGER Spine OCT System	R3531-130	FDA UDI	Class II	Active
TIGER Spine OCT System	R3530-115	FDA UDI	Class II	Active
TIGER Spine System	77365-30	FDA UDI	Class II	Active
FOUNDATION System	MAT0714	FDA UDI	Class II	Active
FOUNDATION System	TM2516	FDA UDI	Class II	Active
ANODYNE Plate System	21352-14	FDA UDI	Class II	Active
CoreLink Foundation 3D Stand Alone Screw	10365-30	FDA UDI	Class II	Active
FLXfit 15	AT4010	FDA UDI	Class II	Active
ANODYNE Plate System	20140-18	FDA UDI	Class II	Active
TIGER Spine OCT System	R3500-050	FDA UDI	Class II	Active
ANODYNE Plate System	20140-15	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.