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Altus Spine

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
Address: —
Website: —
LinkedIn: —
Facebook: —
Email: —
Phone: —
PRRC Contact: —
EUDAMED SRN: —
FDA FEI Number: —
DUNS Number: —

Catalogue (5998)

Page 101 of 120

Device	Model / Reference	Registries	Class	Status
Monaco Pedicle Screw System	922-6165	FDA UDI	Class II	Active
Brickyard	1020-38271216	FDA UDI	Class II	Active
Brickyard Stand-Alone ALIF	1030-0310	FDA UDI	Class I	Active
Valencia Pedicle Screw System	973-4550	FDA UDI	Class II	Active
Brickyard ALIF	FA38271615T	FDA UDI	Class II	Active
Valencia Pedicle Screw System	925-7550	FDA UDI	Class II	Unknown
Valencia Pedicle Screw System	970-5545	FDA UDI	Class II	Active
Brickyard Stand-Alone ALIF	1030-0225	FDA UDI	Class II	Active
Brickyard	1020-34261215	FDA UDI	Class II	Active
Silverstone Titanium Interbody Fusion System	SP221016T	FDA UDI	Class II	Active
Indy Standalone	SL32241211	FDA UDI	Class II	Active
Valencia Pedicle Screw System	990-8590	FDA UDI	Class II	Active
Valencia Pedicle Screw System	975-7525	FDA UDI	Class II	Active
Valencia Pedicle Screw System	973-7555	FDA UDI	Class II	Active
Silverstone Interbody Fusion System	SP221009	FDA UDI	Class II	Active
Monaco Uni-Planar	813-7610	FDA UDI	Class II	Active
Sochi	A16-32-4507	FDA UDI	Class II	Active
Monaco Pedicle Screw System	811-7570	FDA UDI	Class II	Active
Valencia Pedicle Screw System	975-6550	FDA UDI	Class II	Active
Valencia Pedicle Screw System	975-4560	FDA UDI	Class II	Active
Indy Standalone	1030-0300G-45	FDA UDI	Class II	Active
Sochi	A16-12-4528	FDA UDI	Class II	Active
Sochi	A16-21-0206	FDA UDI	Class II	Active
Valencia Pedicle Screw System	943-8545	FDA UDI	Class II	Active
Indy Standalone	SL38271217	FDA UDI	Class II	Active
Brickyard ALIF	FA34261617T	FDA UDI	Class II	Active
Fuji Cervical Plate System	139-4012	FDA UDI	Class II	Active
Altus Spine HA Pedicle Screw System	822-8600HA	FDA UDI	Class II	Active
Indy	1030-38272014	FDA UDI	Class II	Active
Indy	1030-0040	FDA UDI	Class I	Active
Indy	FA34261210T	FDA UDI	Class II	Active
Imola-Silverstone	1000-0705	FDA UDI	Class II	Active
Imola Interbody Fusion System	F63055-08	FDA UDI	Class II	Active
Altus Spine Pedicle Screw System	880-1013	FDA UDI	Class II	Active
Imola Interbody Fusion System	FA122838-14	FDA UDI	Class II	Active
Valencia Pedicle Screw System	909-0480NT	FDA UDI	Class II	Active
Monaco Pedicle Screw System	922-6050	FDA UDI	Class II	Active
Valencia Pedicle Screw System	942-6550	FDA UDI	Class II	Unknown
Brickyard Stand-Alone ALIF	SL38271218T	FDA UDI	Class II	Active
Valencia Pedicle Screw System	960-5525	FDA UDI	Class II	Unknown
Valencia Pedicle Screw System	990-6530	FDA UDI	Class II	Active
Silverstone Titanium Interbody Fusion System	ST52813T	FDA UDI	Class II	Active
Monaco Uni-Planar	813-9620	FDA UDI	Class II	Active
Indy Standalone	SL38272518T	FDA UDI	Class II	Active
Monaco Pedicle Screw System	822-7560	FDA UDI	Class II	Active
Brickyard ALIF	FA34262018	FDA UDI	Class II	Active
Indy	FA34261219	FDA UDI	Class II	Active
Brickyard	1030-2520	FDA UDI	Class I	Active
Indy Standalone	1030-2115A	FDA UDI	Class I	Active
Indy Standalone	SL32242516	FDA UDI	Class II	Active

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