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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 26 of 120

Device	Model / Reference	Registries	Class	Status
Fuji Cervical Plate System	100-1010	FDA UDI	Class II	Active
Altus Spine Cervical Interbody Fusion System	210-1008	FDA UDI	Class II	Active
Monaco Pedicle Screw System	811-7540	FDA UDI	Class II	Active
Valencia Pedicle Screw System	923-5105	FDA UDI	Class II	Active
Monaco Uni-Planar	831-1301	FDA UDI	Class II	Active
Brickyard ALIF	FA32240810	FDA UDI	Class II	Active
Brickyard	1020-38272518	FDA UDI	Class II	Active
Valencia Pedicle Screw System	990-4540	FDA UDI	Class II	Active
Indy	FA38272519	FDA UDI	Class II	Active
Indy	FA34260816	FDA UDI	Class II	Active
Brickyard ALIF	FA38271617	FDA UDI	Class II	Active
Brickyard	1020-34261217	FDA UDI	Class II	Active
Suzuka Interbody Fusion System	S730504	FDA UDI	Class II	Active
Valencia Pedicle Screw System	930-7540	FDA UDI	Class II	Active
Silverstone Interbody Fusion System	PS-301009	FDA UDI	Class II	Active
Valencia Pedicle Screw System	970-7575	FDA UDI	Class II	Active
Imola Interbody Fusion System	F02660-12	FDA UDI	Class II	Active
Suzuka Interbody Fusion System	ALR17-807	FDA UDI	Class II	Active
Brickyard ALIF	FA34262014	FDA UDI	Class II	Active
Monaco Pedicle Screw System	822-9550	FDA UDI	Class II	Active
Brickyard ALIF	FA42300818T	FDA UDI	Class II	Active
Indy	1030-32242020	FDA UDI	Class II	Active
Valencia Pedicle Screw System	973-8585	FDA UDI	Class II	Active
Imola Interbody Fusion System	F02260-08	FDA UDI	Class II	Active
Indy	FA34260811	FDA UDI	Class II	Active
Valencia Pedicle Screw System	973-6550	FDA UDI	Class II	Active
Brickyard Stand-Alone ALIF	SL32241611T	FDA UDI	Class II	Active
Brickyard Stand-Alone ALIF	SL42300820T	FDA UDI	Class II	Active
Imola Interbody Fusion System	FA082838-12	FDA UDI	Class II	Active
Indy	FA38272516	FDA UDI	Class II	Active
Altus Spine Pedicle Screw System	981-0005TN	FDA UDI	Class II	Active
Monaco Pedicle Screw System	931-5160	FDA UDI	Class II	Active
Imola-Silverstone	707-1016	FDA UDI	Class II	Active
Valencia Pedicle Screw System	970-4555	FDA UDI	Class II	Active
Brickyard	1030-32241614	FDA UDI	Class II	Active
Brickyard Stand-Alone ALIF	1030-3015	FDA UDI	Class I	Active
Monaco Pedicle Screw System	912-5120	FDA UDI	Class II	Active
Indy Standalone	SL38271213T	FDA UDI	Class II	Active
Imola Titanium Interbody Fusion System	F01855-12T	FDA UDI	Class II	Active
Fuji Cervical Plate System	121-4022	FDA UDI	Class II	Active
Valencia Pedicle Screw System	905-0007	FDA UDI	Class II	Active
Monaco Pedicle Screw System	911-5140	FDA UDI	Class II	Active
Valencia Pedicle Screw System	980-8545	FDA UDI	Class II	Active
Imola Interbody Fusion System	FA122634-14	FDA UDI	Class II	Active
Brickyard ALIF	FA42301614T	FDA UDI	Class II	Active
Brickyard Stand-Alone ALIF	1030-4010	FDA UDI	Class I	Active
Imola Titanium Interbody Fusion System	F12250-10T	FDA UDI	Class II	Active
Brickyard ALIF	FA42301213T	FDA UDI	Class II	Active
Altus Spine HA Pedicle Screw System	822-9570HA	FDA UDI	Class II	Active
Brickyard ALIF	FA32240809	FDA UDI	Class II	Active

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