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Alliance Partners LLC

United StatesFDA applicant, unverified

Alliance Partners LLC is a medical device manufacturer, with 548 devices listed in FDA GUDID and FDA 510(k) (FDA Class II and I) and 1 FDA recall as of 12 Nov 2026.

Devices
548
FDA recalls
1

Registry facts

Counted by deviCERTS from registry records, 12 Nov 2026

Registries
  • FDA GUDID 538
  • FDA 510(k) 10

A device listed in two registries counts in both.

Device classes
  • FDA Class II 301
  • FDA Class I 247
FDA recalls
Identifiers
  • DUNS 962768169

At a glance

Counted by deviCERTS from registry records

Market reach

United States
FDA recalls

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.

AI-generated from registry data, 26 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue548

Newest first, rows 1-50 of 548

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  • Nakoma ACP System 3100I-7000

    Active Regimes: 510(k) Registry: GUDID Class:II

  • Alamo P 2100T-2714

    Active Regimes: 510(k) Registry: GUDID Class:I

  • Alamo C Interbody Fusion Device 2016I-011

    Active Regimes: 510(k) Registry: GUDID Class:II

  • Alamo C 2016T-206

    Active Regimes: 510(k) Registry: GUDID Class:I

  • Nakoma-SL ACP System 3100I-2001

    Active Regimes: 510(k) Registry: GUDID Class:II

  • Alamo P 2100T-2911

    Active Regimes: 510(k) Registry: GUDID Class:I

  • Alamo T 2811T-1005

    Active Regimes: 510(k) Registry: GUDID Class:I

  • Alamo C 1714T-209

    Active Regimes: 510(k) Registry: GUDID Class:I

  • Alamo C 2016T-212

    Active Regimes: 510(k) Registry: GUDID Class:I

  • Alamo C Interbody Fusion Device 2016I-706

    Active Regimes: 510(k) Registry: GUDID Class:II

  • Alamo C Interbody Fusion Device 1412I-009

    Active Regimes: 510(k) Registry: GUDID Class:II

  • Alamo C 1714T-203

    Active Regimes: 510(k) Registry: GUDID Class:I

  • Alamo P 2100T-2209

    Active Regimes: 510(k) Registry: GUDID Class:I

  • Nakoma-SL ACP System 3100I-5006

    Active Regimes: 510(k) Registry: GUDID Class:II

  • Alamo C 2016T-211

    Active Regimes: 510(k) Registry: GUDID Class:I

  • Alamo C 0107-1409

    Active Regimes: 510(k) Registry: GUDID Class:II

  • Alamo C 0107-1408

    Active Regimes: 510(k) Registry: GUDID Class:II

  • Alamo C 1412T-213

    Active Regimes: 510(k) Registry: GUDID Class:I

  • Alamo C 1714T-214-S

    Active Regimes: 510(k) Registry: GUDID Class:I

  • Alamo P, Alamo T 2100T-1711

    Active Regimes: 510(k) Registry: GUDID Class:I

  • Nakoma 3100T-2400

    Listed Registry: GUDID Class:I

  • Alamo C 0100-1412

    Active Regimes: 510(k) Registry: GUDID Class:II

  • Alamo C Interbody Fusion Device 1714I-712

    Active Regimes: 510(k) Registry: GUDID Class:II

  • Alamo T Interbody Fusion Device 2811I-007

    Active Regimes: 510(k) Registry: GUDID Class:II

  • Alamo C Interbody Fusion Device 1714I-008

    Active Regimes: 510(k) Registry: GUDID Class:II

  • Nakoma-SL ACP System 3100I-1004

    Active Regimes: 510(k) Registry: GUDID Class:II

  • Alamo P 2811T-1002

    Active Regimes: 510(k) Registry: GUDID Class:I

  • Alamo P 2100T-2214

    Active Regimes: 510(k) Registry: GUDID Class:I

  • Alamo C 2016T-209-S

    Active Regimes: 510(k) Registry: GUDID Class:I

  • Alamo P 2100T-3210

    Listed Registry: GUDID Class:I

  • Nakoma ACP System 3100I-6005

    Active Regimes: 510(k) Registry: GUDID Class:II

  • Alamo T 2100T-2806

    Active Regimes: 510(k) Registry: GUDID Class:I

  • RAAS Cranial Plating System 2900I-1081

    Withdrawn Registry: GUDID Class:II

  • Alamo P 2100T-2409

    Active Regimes: 510(k) Registry: GUDID Class:I

  • Nakoma ACP System 3100I-8000

    Active Regimes: 510(k) Registry: GUDID Class:II

  • Alamo T Interbody Fusion Device 3211I-009

    Active Regimes: 510(k) Registry: GUDID Class:II

  • Alamo P 2100T-2614

    Active Regimes: 510(k) Registry: GUDID Class:I

  • Nakoma-SL ACP System 3100I-1005

    Active Regimes: 510(k) Registry: GUDID Class:II

  • Alamo C 1412T-209-S

    Active Regimes: 510(k) Registry: GUDID Class:I

  • Nakoma-SL ACP System 3100I-4001

    Active Regimes: 510(k) Registry: GUDID Class:II

  • Alamo P Interbody Fusion Device 2210I-014

    Active Regimes: 510(k) Registry: GUDID Class:II

  • Alamo T 2100T-3007

    Active Regimes: 510(k) Registry: GUDID Class:I

  • RAAS Cranial Plating System 2900I-1111

    Withdrawn Registry: GUDID Class:II

  • Alamo T 2100T-3310

    Active Regimes: 510(k) Registry: GUDID Class:I

  • Alamo C 0107-1709

    Active Regimes: 510(k) Registry: GUDID Class:II

  • Alamo C 1714T-214

    Active Regimes: 510(k) Registry: GUDID Class:I

  • Alamo P Interbody Fusion Device 2810I-713

    Active Regimes: 510(k) Registry: GUDID Class:II

  • Alamo C 1714T-211

    Active Regimes: 510(k) Registry: GUDID Class:I

  • Alamo C 2016T-210-S

    Active Regimes: 510(k) Registry: GUDID Class:I

  • Alamo C Interbody Fusion Device 1714I-708

    Active Regimes: 510(k) Registry: GUDID Class:II

Rows 1-50 of 548

Showing 1-50 of 548

Company details

DUNS number
962768169
Phone
+1(210)314-2525

FDA recalls1

Recalls are matched to the firm by name. FDA recall data as of 1 Nov 2026.

FDA recall records list 1 recall initiated by ALLIANCE PARTNERS LLC, initiated on 2015-06-09. By recorded status: 1 terminated. The reasons filed fall into these groups: other reasons as filed. A recall is often a precaution started by the manufacturer, and a count of records is not a verdict on a company.

Generated automatically from FDA recall records, as a summary of the records listed below. It describes what the records state and is not an assessment of this manufacturer.

  • 2015

    • 9 Jun 2015 Z-1989-2015 Class II 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. Distribution: US Nationwide Distribution in the states LA, TX, and PR. Submission number: K141993

Frequently asked questions

How many devices does ALLIANCE PARTNERS LLC have in the registry?

The registry currently lists 548 devices for ALLIANCE PARTNERS LLC. Devices recorded under merged duplicate company entries are counted once.

Which registries list ALLIANCE PARTNERS LLC's devices?

Among its 50 most recently registered devices, ALLIANCE PARTNERS LLC has devices listed in FDA GUDID (50 devices).

What risk classes do ALLIANCE PARTNERS LLC's devices fall under?

Among its 50 most recently registered devices, the classes recorded for ALLIANCE PARTNERS LLC's devices are Class I and Class II. Each device page shows its own class and authorisation.

Are there FDA recall records for ALLIANCE PARTNERS LLC?

FDA recall records list 1 recall initiated by ALLIANCE PARTNERS LLC, the most recent initiated on 9 Jun 2015. A recall is often a precaution started by the manufacturer; the records say nothing about the company's overall record.

What are the newest devices from ALLIANCE PARTNERS LLC in the registry?

The most recently registered devices listed for ALLIANCE PARTNERS LLC include Nakoma ACP System 3100I-7000, Alamo P 2100T-2714, Alamo C Interbody Fusion Device 2016I-011 and Alamo C 2016T-206.

Generated automatically from registry data and not verified by a human reviewer.