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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

Country
US
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Catalogue (5998)

Page 33 of 120
DeviceModel / ReferenceRegistriesClassStatus
Brickyard Stand-Alone ALIF 1030-0240G-45
FDA UDI
Class IIActive
Altus Spine HA Pedicle Screw System 811-5060HA
FDA UDI
Class IIActive
Valencia Pedicle Screw System 943-5570
FDA UDI
Class IIActive
Silverstone Titanium Interbody Fusion System ST82809T2
FDA UDI
Class IIActive
Brickyard ALIF FA42300820
FDA UDI
Class IIActive
Valencia Pedicle Screw System 905-0035
FDA UDI
Class IIActive
Indy FA34261220T
FDA UDI
Class IIActive
Sochi A16-18-1050
FDA UDI
Class IIActive
Indy 1020-1220
FDA UDI
Class IIActive
Indy 1030-1213
FDA UDI
Class IActive
Suzuka Interbody Fusion System S410510
FDA UDI
Class IIActive
Imola-Silverstone 600-3109
FDA UDI
Class IIActive
Indy Standalone SL42302517T
FDA UDI
Class IIActive
Monaco Pedicle Screw System 912-6120
FDA UDI
Class IIActive
Indy Standalone SL32240813T
FDA UDI
Class IIActive
Brickyard ALIF FA42300813
FDA UDI
Class IIActive
Imola Interbody Fusion System FA152634-16
FDA UDI
Class IIActive
Imola Interbody Fusion System F12260-10
FDA UDI
Class IIActive
Indy 1030-1116
FDA UDI
Class IActive
Fuji Cervical Plate System 137-4016
FDA UDI
Class IIActive
Brickyard ALIF FA32242516T
FDA UDI
Class IIActive
Fuji Cervical Plate System 114-0486
FDA UDI
Class IIActive
Valencia Pedicle Screw System 925-5540
FDA UDI
Class IIUnknown
Indy 1030-0814
FDA UDI
Class IActive
Monaco Pedicle Screw System 822-8540
FDA UDI
Class IIActive
Altus Spine HA Pedicle Screw System 811-8530HA
FDA UDI
Class IIActive
Valencia Pedicle Screw System 940-5545
FDA UDI
Class IIActive
Imola Interbody Fusion System F63045-08
FDA UDI
Class IIActive
Indy 1030-1219
FDA UDI
Class IActive
PEEK Interbody Fusion System TL22012
FDA UDI
Class IIActive
Indy FA42301620
FDA UDI
Class IIActive
Monaco Pedicle Screw System 922-6035
FDA UDI
Class IIActive
Brickyard Stand-Alone ALIF SL32240815T
FDA UDI
Class IIActive
Brickyard Stand-Alone ALIF SL38271216
FDA UDI
Class IIActive
Indy Standalone SL32240820
FDA UDI
Class IIActive
Monaco Uni-Planar 813-8600
FDA UDI
Class IIActive
Valencia Pedicle Screw System 993-6550
FDA UDI
Class IIActive
Fuji Cervical Plate System 114-0124
FDA UDI
Class IIActive
Valencia Pedicle Screw System 944-0050
FDA UDI
Class IIUnknown
Imola Interbody Fusion System F13060-12
FDA UDI
Class IIActive
Valencia Pedicle Screw System 970-6550
FDA UDI
Class IIActive
Indy 1020-42300812
FDA UDI
Class IIActive
Indy 1020-32241218
FDA UDI
Class IIActive
Indy FA34262014
FDA UDI
Class IIActive
Monaco Pedicle Screw System 932-6050
FDA UDI
Class IIActive
Valencia Pedicle Screw System 970-4550
FDA UDI
Class IIActive
Monaco Pedicle Screw System 901-6040
FDA UDI
Class IIActive
Valencia Pedicle Screw System 940-8580
FDA UDI
Class IIActive
Brickyard ALIF FA34261618
FDA UDI
Class IIActive
Indy 1020-42300816
FDA UDI
Class IIActive

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