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 71 of 72

Device	Model / Reference	Registries	Class	Status
TIGER Spine OCT System	RN3500	FDA UDI	Class II	Active
CoreLink Foundation 3D ALIF Stand-Alone Cage	3AS2535-1516	FDA UDI	Class II	Active
CoreLink Foundation 3D ALIF Stand-Alone Cage	3AS2540-1511	FDA UDI	Class II	Active
CoreLink Foundation 3D ALIF Stand-Alone Cage	3AS2740-1520	FDA UDI	Class II	Active
CoreLink Foundation 3D ALIF Stand-Alone Cage	3AS2540-2020	FDA UDI	Class II	Active
TIGER Spine OCT System	TC3645-51	FDA UDI	Class II	Active
TIGER Spine OCT System	R3512-060	FDA UDI	Class II	Active
CoreLink Foundation 3D Lateral Cage	3LL2255-1210	FDA UDI	Class II	Active
CoreLink Foundation 3D ALIF Stand-Alone Cage	3AS3045-1521	FDA UDI	Class II	Active
CoreLink Foundation 3D Lateral Cage	3LL1845-1214	FDA UDI	Class II	Active
CoreLink 3D Lateral Cage	3LL1855-2014	FDA UDI	Class II	Active
CoreLink 3D Lateral Cage	3LL2255-2516	FDA UDI	Class II	Active
TIGER Spine OCT System	35040-30	FDA UDI	Class II	Active
CoreLink Foundation 3D ALIF Stand-Alone Cage	3AS3040-0811	FDA UDI	Class II	Active
CoreLink 3D Lateral Cage	3LL1840-0012	FDA UDI	Class II	Active
TIGER Spine OCT System	R3512-035	FDA UDI	Class II	Active
TIGER Spine OCT System	35745-24	FDA UDI	Class II	Active
TIGER Spine OCT System	35040-26	FDA UDI	Class II	Active
CoreLink Foundation 3D ALIF Stand-Alone Cage	3AS2735-0821	FDA UDI	Class II	Active
CoreLink LATERAL SCREW	90760-50	FDA UDI	Class II	Active
TIGER Spine OCT System	35040-12	FDA UDI	Class II	Active
CoreLink 3D Lateral Cage	3LL2235-0010	FDA UDI	Class II	Active
CoreLink Foundation 3D ALIF Stand-Alone Cage	3AS3045-0818	FDA UDI	Class II	Active
CoreLink Foundation 3D ALIF Stand-Alone Cage	3AS3045-2519	FDA UDI	Class II	Active
TIGER Spine OCT System	35940-34	FDA UDI	Class II	Active
CoreLink Foundation 3D ALIF Stand-Alone Cage	3AS2740-2015	FDA UDI	Class II	Active
TIGER Spine OCT System	R3555-420	FDA UDI	Class II	Active
TIGER Spine OCT System	35735-22	FDA UDI	Class II	Active
TIGER Spine OCT System	35045-32	FDA UDI	Class II	Active
TIGER Spine OCT System	35840-34	FDA UDI	Class II	Active
CoreLink Foundation 3D ALIF Stand-Alone Cage	3AS2535-1514	FDA UDI	Class II	Active
CoreLink Foundation 3D ALIF Stand-Alone Cage	3AS2735-2014	FDA UDI	Class II	Active
CoreLink Foundation 3D ALIF Stand-Alone Cage	3AS3045-2515	FDA UDI	Class II	Active
CoreLink Foundation 3D Lateral Cage	3LL2260-1210	FDA UDI	Class II	Active
TIGER Spine OCT System	R3531-145	FDA UDI	Class II	Active
TIGER Spine OCT System	35945-34	FDA UDI	Class II	Active
CoreLink Foundation 3D ALIF Stand-Alone Cage	3AS2735-2519	FDA UDI	Class II	Active
CoreLink 3D Lateral Cage	3LL2255-0012	FDA UDI	Class II	Active
CoreLink 3D Lateral Cage	3LL2250-3016	FDA UDI	Class II	Active
CoreLink Foundation 3D ALIF Stand-Alone Cage	3AS3045-1516	FDA UDI	Class II	Active
CoreLink Foundation 3D Lateral Cage	3LL1855-1214	FDA UDI	Class II	Active
CoreLink 3D Lateral Cage	3LL2250-3020	FDA UDI	Class II	Active
CoreLink 3D Lateral Cage	3LL2250-2016	FDA UDI	Class II	Active
TIGER Spine OCT System	35040-44	FDA UDI	Class II	Active
TIGER Spine OCT System	35035-20	FDA UDI	Class II	Active
TIGER Spine OCT System	35040-40	FDA UDI	Class II	Active
CoreLink LATERAL SCREW	900415-22	FDA UDI	Class II	Active
CoreLink Foundation 3D ALIF Stand-Alone Cage	3AS2735-0816	FDA UDI	Class II	Active
FLXfit 15	AT4009	FDA UDI	Class II	Active
CoreLink 3D Lateral Cage	3LL2260-2516	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.