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Sign in to claim this brandALLIANCE PARTNERS LLC
US
Last updated May 24, 2026
What ALLIANCE PARTNERS LLC makes
Alliance Partners LLC manufactures reusable orthopaedic surgical instruments, including bone files, rasps, curettes, knives, and fluted drill bits for spinal procedures. Their product portfolio also includes non-bioabsorbable spinal fixation plates and polymeric spinal interbody fusion cages designed for intervertebral fusion trials. These devices are intended for use in spinal surgeries to stabilize vertebrae and facilitate bone healing.
The company’s devices are classified under FDA’s Class I and Class II categories and are listed in the FDA’s Unique Device Identifier (UDI) database. Alliance Partners LLC is based in the United States.
Written from this company's registered devices by an AI model, and not verified by a human reviewer.
Frequently asked questions
What types of medical devices does Alliance Partners LLC manufacture?
Alliance Partners LLC specializes in reusable orthopaedic surgical instruments and spinal implants. Their product line includes bone files, rasps, curettes, knives, and fluted surgical drill bits, which are used during spinal procedures. They also produce non-bioabsorbable spinal fixation plates and polymeric spinal interbody fusion cages, designed specifically for intervertebral fusion trials to stabilize vertebrae and promote bone healing.
Where is Alliance Partners LLC based?
Alliance Partners LLC is headquartered in the United States. Their location is relevant for understanding regulatory compliance and distribution, as their devices are intended for use in spinal surgeries within the US market.
Which regulatory registries list Alliance Partners LLC’s devices?
Alliance Partners LLC’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry helps track and identify medical devices by assigning a standardized identifier, ensuring traceability and compliance with regulatory requirements.
How are Alliance Partners LLC’s devices classified under FDA regulations?
Alliance Partners LLC’s devices fall under FDA’s Class I and Class II categories. Class I devices generally pose the lowest risk and may require less regulatory oversight, while Class II devices involve moderate risk and require special controls to ensure safety and effectiveness. The classification depends on factors like the device’s intended use and potential risks.
What is the purpose of the spinal implants and instruments manufactured by Alliance Partners LLC?
The spinal implants and instruments produced by Alliance Partners LLC are designed for spinal surgeries. The reusable instruments, such as bone files and fluted drill bits, assist surgeons in preparing the spine for fusion procedures. The spinal fixation plates and interbody fusion cages, like the Alamo and Nakoma systems, are intended to stabilize vertebrae and facilitate bone fusion, helping patients recover structural integrity and mobility after spinal interventions.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- —
- Website
- alliance-spine.com
- —
- —
- [email protected]
- Phone
- +1(210)314-2525
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 962768169
Catalogue (548)
Page 10 of 11| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Nakoma ACP System | 3100I-8006 | FDA UDI | Class II | Active |
| Nakoma | 3100T-1800 | FDA UDI | Class I | Active |
| RAAS Cranial Plating System | 2900I-1060 | FDA UDI | Class II | Unknown |
| Alamo C | 2016T-207-S | FDA UDI | Class I | Active |
| Alamo P | 2100T-2212 | FDA UDI | Class I | Active |
| RAAS Cranial Plating System | 2900I-1050 | FDA UDI | Class II | Unknown |
| Alamo P Interbody Fusion Device | 2810I-014 | FDA UDI | Class II | Active |
| Alamo P | 2100T-3110 | FDA UDI | Class I | Active |
| RAAS Cranial Plating System | 2900I-1121 | FDA UDI | Class II | Unknown |
| Alamo P Interbody Fusion Device | 2810I-009 | FDA UDI | Class II | Active |
| Alamo P, Alamo T | 2100T-1610 | FDA UDI | Class I | Active |
| Nakoma ACP System | 3100I-7008 | FDA UDI | Class II | Active |
| Nakoma ACP System | 3100I-9009 | FDA UDI | Class II | Active |
| Alamo P Interbody Fusion Device | 2210I-709 | FDA UDI | Class II | Active |
| Alamo P Interbody Fusion Device | 2510I-013 | FDA UDI | Class II | Active |
| Alamo P Interbody Fusion Device | 2810I-709 | FDA UDI | Class II | Active |
| Alamo C | 1714T-207-S | FDA UDI | Class I | Active |
| Alamo P | 2100T-2211 | FDA UDI | Class I | Active |
| Nakoma ACP System | 3100I-9001 | FDA UDI | Class II | Active |
| Alamo T Interbody Fusion Device | 3211I-011 | FDA UDI | Class II | Active |
| Nakoma ACP System | 3100I-8005 | FDA UDI | Class II | Active |
| Alamo T Interbody Fusion Device | 3211I-008 | FDA UDI | Class II | Active |
| Alamo T | 2100T-2812 | FDA UDI | Class I | Active |
| Alamo C | 0100-1705 | FDA UDI | Class II | Active |
| Alamo C | 1412T-214 | FDA UDI | Class I | Active |
| Alamo P Interbody Fusion Device | 2210I-713 | FDA UDI | Class II | Active |
| Alamo P Interbody Fusion Device | 2810I-711 | FDA UDI | Class II | Active |
| Alamo C Interbody Fusion Device | 1412I-006 | FDA UDI | Class II | Active |
| Alamo T Interbody Fusion Device | 2811I-011 | FDA UDI | Class II | Active |
| Alamo P, Alamo T | 2100T-2100 | FDA UDI | Class I | Active |
| Nakoma ACP System | 3100I-7002 | FDA UDI | Class II | Active |
| Alamo P, Alamo T | 2100T-1710 | FDA UDI | Class I | Active |
| Alamo P | 2100T-3112 | FDA UDI | Class I | Active |
| Nakoma ACP System | 3100I-7500 | FDA UDI | Class II | Active |
| Nakoma-SL ACP System | 3100I-5003 | FDA UDI | Class II | Active |
| Alamo C | 1714T-200 | FDA UDI | Class I | Active |
| Alamo T | 2100T-3012 | FDA UDI | Class I | Active |
| Alamo C Interbody Fusion Device | 2016I-709 | FDA UDI | Class II | Active |
| Alamo P | 2100T-2208 | FDA UDI | Class I | Active |
| Alamo C | 0100-1410 | FDA UDI | Class II | Active |
| Alamo C | 0100-1710 | FDA UDI | Class II | Active |
| Nakoma-SL ACP System | 3100I-3001 | FDA UDI | Class II | Active |
| Alamo C Interbody Fusion Device | 1714I-710 | FDA UDI | Class II | Active |
| Alamo P Interbody Fusion Device | 2210I-012 | FDA UDI | Class II | Active |
| Alamo P | 2100T-2310 | FDA UDI | Class I | Active |
| Alamo T Interbody Fusion Device | 2811I-008 | FDA UDI | Class II | Active |
| Alamo P | 2100T-2713 | FDA UDI | Class I | Active |
| Nakoma ACP System | 3100I-8008 | FDA UDI | Class II | Active |
| Alamo C | 1714T-201 | FDA UDI | Class I | Active |
| Alamo P | 2100T-2710 | FDA UDI | Class I | Active |
Related Companies
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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.
Alliance Partners LLC has one FDA recall record initiated on 2015-06-09, which is marked as terminated. The recall was due to a potential issue where the screw and plate design may allow the screw to advance through the plate if implanted at an angle greater than 7 degrees.
AI-generated summary of the recall records listed below. It describes what the records state and is not an assessment of this manufacturer.
| 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. |