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Altus Spine

US

Last updated May 23, 2026

What Altus Spine makes

Altus Spine manufactures spinal implants and orthopaedic fixation devices, including non-bioabsorbable bone screws, metallic and polymeric interbody fusion cages, spinal fixation plates, and internal spinal fixation rods. Their portfolio also includes spinal implant trial systems, reusable orthopaedic surgical procedure kits, and internal spinal distractors for surgical procedures.

The company’s devices are classified under FDA categories Class I and Class II, with listings in the FDA’s Unique Device Identifier (UDI) database. Altus Spine 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 Altus Spine manufacture?

Altus Spine specializes in spinal implants and orthopaedic fixation devices. Their product portfolio includes non-bioabsorbable bone screws, metallic and polymeric interbody fusion cages, spinal fixation plates, internal spinal fixation rods, spinal implant trial systems, reusable orthopaedic surgical procedure kits, and internal spinal distractors. These devices are designed for spinal surgeries and orthopaedic procedures.

Where is Altus Spine based?

Altus Spine is headquartered in the United States. The company’s location is relevant for understanding its regulatory framework and compliance with U.S. medical device regulations.

Which regulatory registries list Altus Spine’s devices?

Altus Spine’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry helps track and identify medical devices authorized for use in the U.S., ensuring transparency and traceability in the healthcare system.

How are Altus Spine’s devices classified under FDA regulations?

Altus Spine’s devices fall under two FDA classification categories: Class I and Class II. Class I devices generally pose the lowest risk and may require general controls, while Class II devices involve moderate risk and require special controls to ensure safety and effectiveness. Classification depends on factors like the device’s intended use and potential health impact.

AI-generated from registry data and not verified by a human reviewer.

Information

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US
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Catalogue (5998)

Page 20 of 120
DeviceModel / ReferenceRegistriesClassStatus
Silverstone Titanium Interbody Fusion System ST03214T2
FDA UDI
Class IIActive
Fuji Cervical Plate System 114-0247
FDA UDI
Class IIActive
Fuji Cervical Plate System 139-4016
FDA UDI
Class IIActive
Indy 1020-32242013
FDA UDI
Class IIActive
Valencia Pedicle Screw System 983-8555
FDA UDI
Class IIActive
Indy Standalone SL38270820T
FDA UDI
Class IIActive
Imola Titanium Interbody Fusion System F13050-10T
FDA UDI
Class IIActive
Valencia Pedicle Screw System 980-7550
FDA UDI
Class IIActive
Sochi A16-23-5520
FDA UDI
Class IIActive
Indy FA34260819T
FDA UDI
Class IIActive
Monaco Uni-Planar 831-1002
FDA UDI
Class IIActive
Brickyard Stand-Alone ALIF 1030-3235G-45
FDA UDI
Class IActive
Indy FA34262517
FDA UDI
Class IIActive
Silverstone Interbody Fusion System SP301010
FDA UDI
Class IIActive
Imola Titanium Interbody Fusion System F02650-14T
FDA UDI
Class IIActive
Monaco Uni-Planar 813-5550
FDA UDI
Class IIActive
Suzuka Interbody Fusion System S731011T
FDA UDI
Class IIActive
Suzuka Interbody Fusion System ALR528
FDA UDI
Class IIActive
Valencia Pedicle Screw System 973-5560
FDA UDI
Class IIActive
Brickyard ALIF FA32241219T
FDA UDI
Class IIActive
Indy Standalone 1030-2430A
FDA UDI
Class IActive
Indy Standalone SL32240816
FDA UDI
Class IIActive
Sochi A16-32-4009
FDA UDI
Class IIActive
Brickyard Stand-Alone ALIF SL32241215
FDA UDI
Class IIActive
Brickyard 1030-32240811
FDA UDI
Class IIActive
Sochi A16-13-4028
FDA UDI
Class IIActive
Indy Standalone SLV4230
FDA UDI
Class IIActive
Valencia Pedicle Screw System 960-6545
FDA UDI
Class IIUnknown
Indy FA34261616T
FDA UDI
Class IIActive
Indy 1030-2018
FDA UDI
Class IActive
Indy 1020-32242014
FDA UDI
Class IIActive
Indy Standalone SL42300817T
FDA UDI
Class IIActive
Brickyard Stand-Alone ALIF SL32241611
FDA UDI
Class IIActive
Monaco Pedicle Screw System 912-6220
FDA UDI
Class IIActive
Brickyard Stand-Alone ALIF SL38271211T
FDA UDI
Class IIActive
Sochi A16-12-5030
FDA UDI
Class IIActive
Indy 1030-32240816
FDA UDI
Class IIActive
Indy FA32241612T
FDA UDI
Class IIActive
Indy Standalone SL42302518T
FDA UDI
Class IIActive
Monaco Pedicle Screw System 822-7600
FDA UDI
Class IIActive
Silverstone Titanium Interbody Fusion System ST52807T
FDA UDI
Class IIActive
Valencia Pedicle Screw System 925-7540
FDA UDI
Class IIUnknown
Monaco Pedicle Screw System 921-6110
FDA UDI
Class IIActive
Monaco Pedicle Screw System 811-9525
FDA UDI
Class IIActive
Indy 1030-2014
FDA UDI
Class IActive
Brickyard ALIF FA42301220
FDA UDI
Class IIActive
Imola Interbody Fusion System F12650-14
FDA UDI
Class IIActive
Valencia Pedicle Screw System 913-5140
FDA UDI
Class IIActive
Valencia Pedicle Screw System 960-5560
FDA UDI
Class IIUnknown
Valencia Pedicle Screw System 950-7550
FDA UDI
Class IIActive

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