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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 1 of 11

Device	Model / Reference	Registries	Class	Status
Nakoma ACP System	3100I-7000	FDA UDI	Class II	Active
Alamo P	2100T-2714	FDA UDI	Class I	Active
Alamo C Interbody Fusion Device	2016I-011	FDA UDI	Class II	Active
Alamo C	2016T-206	FDA UDI	Class I	Active
Nakoma-SL ACP System	3100I-2001	FDA UDI	Class II	Active
Alamo P	2100T-2911	FDA UDI	Class I	Active
Alamo T	2811T-1005	FDA UDI	Class I	Active
Alamo C	1714T-209	FDA UDI	Class I	Active
Alamo C	2016T-212	FDA UDI	Class I	Active
Alamo C Interbody Fusion Device	2016I-706	FDA UDI	Class II	Active
Alamo C Interbody Fusion Device	1412I-009	FDA UDI	Class II	Active
Alamo C	1714T-203	FDA UDI	Class I	Active
Alamo P	2100T-2209	FDA UDI	Class I	Active
Nakoma-SL ACP System	3100I-5006	FDA UDI	Class II	Active
Alamo C	2016T-211	FDA UDI	Class I	Active
Alamo C	0107-1409	FDA UDI	Class II	Active
Alamo C	0107-1408	FDA UDI	Class II	Active
Alamo C	1412T-213	FDA UDI	Class I	Active
Alamo C	1714T-214-S	FDA UDI	Class I	Active
Alamo P, Alamo T	2100T-1711	FDA UDI	Class I	Active
Nakoma	3100T-2400	FDA UDI	Class I	Active
Alamo C	0100-1412	FDA UDI	Class II	Active
Alamo C Interbody Fusion Device	1714I-712	FDA UDI	Class II	Active
Alamo T Interbody Fusion Device	2811I-007	FDA UDI	Class II	Active
Alamo C Interbody Fusion Device	1714I-008	FDA UDI	Class II	Active
Nakoma-SL ACP System	3100I-1004	FDA UDI	Class II	Active
Alamo P	2811T-1002	FDA UDI	Class I	Active
Alamo P	2100T-2214	FDA UDI	Class I	Active
Alamo C	2016T-209-S	FDA UDI	Class I	Active
Alamo P	2100T-3210	FDA UDI	Class I	Active
Nakoma ACP System	3100I-6005	FDA UDI	Class II	Active
Alamo T	2100T-2806	FDA UDI	Class I	Active
RAAS Cranial Plating System	2900I-1081	FDA UDI	Class II	Unknown
Alamo P	2100T-2409	FDA UDI	Class I	Active
Nakoma ACP System	3100I-8000	FDA UDI	Class II	Active
Alamo T Interbody Fusion Device	3211I-009	FDA UDI	Class II	Active
Alamo P	2100T-2614	FDA UDI	Class I	Active
Nakoma-SL ACP System	3100I-1005	FDA UDI	Class II	Active
Alamo C	1412T-209-S	FDA UDI	Class I	Active
Nakoma-SL ACP System	3100I-4001	FDA UDI	Class II	Active
Alamo P Interbody Fusion Device	2210I-014	FDA UDI	Class II	Active
Alamo T	2100T-3007	FDA UDI	Class I	Active
RAAS Cranial Plating System	2900I-1111	FDA UDI	Class II	Unknown
Alamo T	2100T-3310	FDA UDI	Class I	Active
Alamo C	0107-1709	FDA UDI	Class II	Active
Alamo C	1714T-214	FDA UDI	Class I	Active
Alamo P Interbody Fusion Device	2810I-713	FDA UDI	Class II	Active
Alamo C	1714T-211	FDA UDI	Class I	Active
Alamo C	2016T-210-S	FDA UDI	Class I	Active
Alamo C Interbody Fusion Device	1714I-708	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.