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Sign in to claim this brandAltus 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 115 of 120| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Brickyard | 1030-32242017 | FDA UDI | Class II | Active |
| Indy | FA38270811 | FDA UDI | Class II | Active |
| Suzuka Interbody Fusion System | ALR17-009 | FDA UDI | Class II | Active |
| Indy | 1030-38271614 | FDA UDI | Class II | Active |
| Indy | FA32242518T | FDA UDI | Class II | Active |
| Indy | 1020-38270811 | FDA UDI | Class II | Active |
| Indy | 1030-32242514 | FDA UDI | Class II | Active |
| Indy | FA32241210 | FDA UDI | Class II | Active |
| Indy | FA32242018T | FDA UDI | Class II | Active |
| PEEK Interbody Fusion System | PL010 | FDA UDI | Class II | Active |
| Suzuka Interbody Fusion System | S420006T | FDA UDI | Class II | Active |
| Silverstone Titanium Interbody Fusion System | ST52215 | FDA UDI | Class II | Active |
| Brickyard ALIF | FA32242015T | FDA UDI | Class II | Active |
| Brickyard | 1030-32240810 | FDA UDI | Class II | Active |
| Imola Titanium Interbody Fusion System | F12660-10T | FDA UDI | Class II | Active |
| Brickyard Stand-Alone ALIF | 1030-4007 | FDA UDI | Class I | Active |
| Silverstone Titanium Interbody Fusion System | ST53216T2 | FDA UDI | Class II | Active |
| Indy | FA34262519T | FDA UDI | Class II | Active |
| Silverstone Titanium Interbody Fusion System | SP221010T2 | FDA UDI | Class II | Active |
| Imola-Silverstone | 1000-0450 | FDA UDI | Class II | Active |
| Indy | 1030-38272517 | FDA UDI | Class II | Active |
| Silverstone Interbody Fusion System | PS-261014 | FDA UDI | Class II | Active |
| Imola Titanium Interbody Fusion System | F02640-12T | FDA UDI | Class II | Active |
| Imola Titanium Interbody Fusion System | F02650-10T | FDA UDI | Class II | Active |
| Suzuka Interbody Fusion System | ALR125 | FDA UDI | Class II | Active |
| Indy | 1020-34261219 | FDA UDI | Class II | Active |
| Brickyard ALIF | FA42301211 | FDA UDI | Class II | Active |
| Imola-Silverstone | 707-1011 | FDA UDI | Class II | Active |
| Indy | FA34260810T | FDA UDI | Class II | Active |
| Indy | FA32241214 | FDA UDI | Class II | Active |
| Indy | FA32242514T | FDA UDI | Class II | Active |
| Imola Titanium Interbody Fusion System | F11845-10T | FDA UDI | Class II | Active |
| Suzuka Interbody Fusion System | ALR507 | FDA UDI | Class II | Active |
| Imola Titanium Interbody Fusion System | F01850-08T | FDA UDI | Class II | Active |
| Indy | FA34261612T | FDA UDI | Class II | Active |
| Brickyard ALIF | FA42301618 | FDA UDI | Class II | Active |
| Indy | FA32242017T | FDA UDI | Class II | Active |
| Brickyard Stand-Alone ALIF | SL32242012T | FDA UDI | Class II | Active |
| Indy | FA32241617T | FDA UDI | Class II | Active |
| Suzuka Interbody Fusion System | S410810 | FDA UDI | Class II | Active |
| Silverstone Interbody Fusion System | SEC00932-09 | FDA UDI | Class II | Active |
| Brickyard Stand-Alone ALIF | 1030-0001 | FDA UDI | Class II | Active |
| Imola-Silverstone | 780-0010 | FDA UDI | Class II | Active |
| Indy | 1030-38271213 | FDA UDI | Class II | Active |
| Indy | 1030-1220 | FDA UDI | Class I | Active |
| PSS Pedicle Screw System | 900-1015 | FDA UDI | Class II | Active |
| Indy | 1020-32241620 | FDA UDI | Class II | Active |
| Imola Titanium Interbody Fusion System | F02655-10T | FDA UDI | Class II | Active |
| Brickyard ALIF | FA32242514 | FDA UDI | Class II | Active |
| Indy Standalone | SL42301213T | FDA UDI | Class II | Active |
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