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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 11 of 11

Device	Model / Reference	Registries	Class	Status
Alamo C	1714T-201-S	FDA UDI	Class I	Active
Alamo C	2016T-209	FDA UDI	Class I	Active
Alamo P, Alamo T	2100T-2000	FDA UDI	Class I	Active
Nakoma ACP System	3100I-7505	FDA UDI	Class II	Active
Alamo T	2100T-2807	FDA UDI	Class I	Active
Alamo P	2100T-2314	FDA UDI	Class I	Active
Alamo C	0100-1411	FDA UDI	Class II	Active
Alamo C	2016T-208	FDA UDI	Class I	Active
Alamo C	1714T-204-S	FDA UDI	Class I	Active
Alamo P Interbody Fusion Device	2810I-712	FDA UDI	Class II	Active
Nakoma ACP System	3100I-9003	FDA UDI	Class II	Active
Nakoma ACP System	3100I-9000	FDA UDI	Class II	Active
Nakoma-SL ACP System	3100I-5004	FDA UDI	Class II	Active
Nakoma ACP System	3100I-6003	FDA UDI	Class II	Active
Nakoma ACP System	3100I-6010	FDA UDI	Class II	Active
Alamo C Interbody Fusion Device	2016I-010	FDA UDI	Class II	Active
Nakoma ACP System	3100I-9500	FDA UDI	Class II	Active
Nakoma ACP System	3100I-9007	FDA UDI	Class II	Active
Nakoma ACP System	3100I-6001	FDA UDI	Class II	Active
Nakoma-SL ACP System	3100I-1003	FDA UDI	Class II	Active
Nakoma ACP System	3100I-9502	FDA UDI	Class II	Active
Nakoma ACP System	3100I-7504	FDA UDI	Class II	Active
Alamo C Interbody Fusion Device	1412I-007	FDA UDI	Class II	Active
Alamo C Interbody Fusion Device	1412I-011	FDA UDI	Class II	Active
Alamo C Interbody Fusion Device	2016I-007	FDA UDI	Class II	Active
Alamo P, Alamo T	2100T-1901	FDA UDI	Class I	Active
Alamo P, Alamo T	2100T-1402	FDA UDI	Class I	Active
Alamo P Interbody Fusion Device	2810I-714	FDA UDI	Class II	Active
Alamo C Interbody Fusion Device	1412I-708	FDA UDI	Class II	Active
Nakoma-SL ACP System	3100I-4000	FDA UDI	Class II	Active
Alamo T	2100T-3314	FDA UDI	Class I	Active
Alamo P Interbody Fusion Device	2210I-011	FDA UDI	Class II	Active
Nakoma ACP System	3100I-6501	FDA UDI	Class II	Active
Nakoma ACP System	3100I-7007	FDA UDI	Class II	Active
Alamo P Interbody Fusion Device	2810I-710	FDA UDI	Class II	Active
Alamo P, Alamo T	2100T-1613	FDA UDI	Class I	Active
Nakoma ACP System	3100I-7004	FDA UDI	Class II	Active
Alamo P Interbody Fusion Device	2210I-712	FDA UDI	Class II	Active
Alliance Spine Raas Cranial Plating System	K141123	FDA 510(k)	Class II	Active
Nakoma Acp	K141993	FDA 510(k)	Class II	Active
Alamo C	K133321	FDA 510(k)	Class II	Active
Medina Anterior Cervical Plate System	K201521	FDA 510(k)	Class II	Active
Alamo® C	K133321	FDA 510(k)	Class II	Active
Alamo T	K120401	FDA 510(k)	Class II	Active
Swannshidi Bone Marrow Aspiration Needle	K121181	FDA 510(k)	Class II	Active
Alamo C	K112361	FDA 510(k)	Class II	Active
Alamo T	K140303	FDA 510(k)	Class II	Active
Alamo P	K122047	FDA 510(k)	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.