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ALLIANCE PARTNERS LLC

Last updated May 24, 2026

Information

Country: US
Address: —
Website: alliance-spine.com
LinkedIn: —
Facebook: —
Email: [email protected]
Phone: +1(210)314-2525
PRRC Contact: —
EUDAMED SRN: —
FDA FEI Number: —
DUNS Number: 962768169

Catalogue (548)

Page 3 of 11

Device	Model / Reference	Registries	Class	Status
Alamo C	1412T-215	FDA UDI	Class I	Active
Alamo C Interbody Fusion Device	2016I-710	FDA UDI	Class II	Active
Alamo C	1714T-212	FDA UDI	Class I	Active
Alamo P, Alamo T	2100T-1608	FDA UDI	Class I	Active
Alamo C	1412T-200-S	FDA UDI	Class I	Active
Alamo C Interbody Fusion Device	1714I-706	FDA UDI	Class II	Active
Alamo P	2100T-2412	FDA UDI	Class I	Active
Nakoma ACP System	3100I-9508	FDA UDI	Class II	Active
Alamo P	2100T-3209	FDA UDI	Class I	Active
RAAS Cranial Plating System	2900I-1200	FDA UDI	Class II	Unknown
Nakoma	3100T-1100	FDA UDI	Class I	Active
Nakoma-SL ACP System	3100I-2004	FDA UDI	Class II	Active
Alamo T	2100T-3410	FDA UDI	Class I	Active
Nakoma ACP System	3100I-6508	FDA UDI	Class II	Active
Alamo P Interbody Fusion Device	2810I-008	FDA UDI	Class II	Active
Alamo T Interbody Fusion Device	3211I-010	FDA UDI	Class II	Active
Nakoma ACP System	3100I-6008	FDA UDI	Class II	Active
RAAS Cranial Plating System	2900I-1080	FDA UDI	Class II	Unknown
Alamo C	0100-1407	FDA UDI	Class II	Active
Alamo C Interbody Fusion Device	1412I-010	FDA UDI	Class II	Active
Alamo C	1412T-211	FDA UDI	Class I	Active
Nakoma ACP System	3100I-9507	FDA UDI	Class II	Active
Alamo C	2016T-206-S	FDA UDI	Class I	Active
Alamo C	1412T-201	FDA UDI	Class I	Active
Nakoma	3100T-1200	FDA UDI	Class I	Active
Nakoma ACP System	3100I-6504	FDA UDI	Class II	Active
Alamo P, Alamo T	2100T-1134	FDA UDI	Class I	Active
Nakoma-SL ACP System	3100I-3002	FDA UDI	Class II	Active
Alamo C	1412T-203	FDA UDI	Class I	Active
Alamo P	2100T-3212	FDA UDI	Class I	Active
Alamo C	2016T-214-S	FDA UDI	Class I	Active
Alamo P Interbody Fusion Device	2510I-710	FDA UDI	Class II	Active
Nakoma ACP System	3100I-8503	FDA UDI	Class II	Active
Alamo C	1412T-400	FDA UDI	Class I	Active
Alamo P	2100T-2910	FDA UDI	Class I	Active
Alamo T	2100T-3413	FDA UDI	Class I	Active
Alamo C	0107-1710	FDA UDI	Class II	Active
Nakoma ACP System	3100I-6000	FDA UDI	Class II	Active
Alamo C	1714T-208-S	FDA UDI	Class I	Active
Alamo C Interbody Fusion Device	1412I-008	FDA UDI	Class II	Active
Alamo P	2100T-2608	FDA UDI	Class I	Active
Nakoma-SL ACP System	3100I-5001	FDA UDI	Class II	Active
Alamo P	2100T-2210	FDA UDI	Class I	Active
Alamo C	0107-1708	FDA UDI	Class II	Active
Alamo P	2100T-2613	FDA UDI	Class I	Active
Alamo C	1714T-206	FDA UDI	Class I	Active
Alamo C	1412T-206-S	FDA UDI	Class I	Active
Alamo P	2100T-2308	FDA UDI	Class I	Active
Alamo P Interbody Fusion Device	2210I-710	FDA UDI	Class II	Active
Alamo P Interbody Fusion Device	2210I-008	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
Jun 9, 2015	Z-1989-2015	—	terminated	Inadequate interference between the screw and the plate when screw implanted into the plate at angulation greater than 7 degrees can result in the screw advancing through the plate during implantation.