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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 2 of 11

Device	Model / Reference	Registries	Class	Status
Alamo P Interbody Fusion Device	2510I-011	FDA UDI	Class II	Active
Nakoma ACP System	3100I-9002	FDA UDI	Class II	Active
Alamo C	1412T-211-S	FDA UDI	Class I	Active
Alamo T	2100T-3308	FDA UDI	Class I	Active
Alamo T	2100T-3014	FDA UDI	Class I	Active
Nakoma ACP System	3100I-9501	FDA UDI	Class II	Active
Alamo T	2100T-3312	FDA UDI	Class I	Active
Alamo C Interbody Fusion Device	2016I-006	FDA UDI	Class II	Active
Nakoma	3100T-1700	FDA UDI	Class I	Active
Alamo P, Alamo T	2100T-1714	FDA UDI	Class I	Active
Nakoma-SL ACP System	3100I-3006	FDA UDI	Class II	Active
Alamo C	0100-1405	FDA UDI	Class II	Active
Alamo P, Alamo T	2100T-1104	FDA UDI	Class I	Active
Alamo C	2016T-204-S	FDA UDI	Class I	Active
Alamo C Interbody Fusion Device	1714I-709	FDA UDI	Class II	Active
Alamo P	2100T-2610	FDA UDI	Class I	Active
Alamo P	2100T-2213	FDA UDI	Class I	Active
Alamo P, Alamo T	2100T-1140	FDA UDI	Class I	Active
Nakoma ACP System	3100I-9505	FDA UDI	Class II	Active
RAAS Cranial Plating System	2900I-1202	FDA UDI	Class II	Unknown
RAAS Cranial Plating System	2900I-1040	FDA UDI	Class II	Unknown
Alamo C	2016T-201	FDA UDI	Class I	Active
Alamo C	0100-1707	FDA UDI	Class II	Active
Alamo C	2016T-211-S	FDA UDI	Class I	Active
Alamo P	2100T-2309	FDA UDI	Class I	Active
Nakoma ACP System	3100I-8504	FDA UDI	Class II	Active
Nakoma-SL ACP System	3100I-4004	FDA UDI	Class II	Active
Alamo P Interbody Fusion Device	2810I-010	FDA UDI	Class II	Active
Alamo C	1714T-203-S	FDA UDI	Class I	Active
Nakoma ACP System	3100I-8010	FDA UDI	Class II	Active
Nakoma ACP System	3100I-9010	FDA UDI	Class II	Active
Alamo C Interbody Fusion Device	1412I-005	FDA UDI	Class II	Active
Alamo C	1714T-210-S	FDA UDI	Class I	Active
Alamo C Interbody Fusion Device	1412I-706	FDA UDI	Class II	Active
Alamo P Interbody Fusion Device	2510I-712	FDA UDI	Class II	Active
Alamo C	1412T-210-S	FDA UDI	Class I	Active
Nakoma	3100T-1805	FDA UDI	Class I	Active
Alamo C	0107-1711	FDA UDI	Class II	Active
Alamo C Interbody Fusion Device	1412I-705	FDA UDI	Class II	Active
Alamo C Interbody Fusion Device	2016I-008	FDA UDI	Class II	Active
Alamo C	1714T-215-S	FDA UDI	Class I	Active
Alamo T	2100T-3010	FDA UDI	Class I	Active
Nakoma ACP System	3100I-9005	FDA UDI	Class II	Active
Alamo P, Alamo T	2100T-1801	FDA UDI	Class I	Active
Alamo P Interbody Fusion Device	2210I-714	FDA UDI	Class II	Active
Nakoma ACP System	3100I-9503	FDA UDI	Class II	Active
Alamo C Interbody Fusion Device	1714I-009	FDA UDI	Class II	Active
Nakoma	3100T-1600	FDA UDI	Class I	Active
Nakoma-SL ACP System	3100I-5005	FDA UDI	Class II	Active
Alamo T	2100T-2814	FDA UDI	Class I	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.