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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 30 of 120

Device	Model / Reference	Registries	Class	Status
Valencia Pedicle Screw System	975-4545	FDA UDI	Class II	Active
Valencia Pedicle Screw System	943-5545	FDA UDI	Class II	Active
Altus Spine Pedicle Screw System	981-0004T	FDA UDI	Class II	Active
Monaco Pedicle Screw System	902-6110	FDA UDI	Class II	Active
Monaco Pedicle Screw System	931-5145	FDA UDI	Class II	Active
Brickyard	1030-38270815	FDA UDI	Class II	Active
Indy	FA38272520T	FDA UDI	Class II	Active
Fuji Cervical Plate System	138-4020	FDA UDI	Class II	Active
Imola Titanium Interbody Fusion System	F02660-08T	FDA UDI	Class II	Active
Monaco Pedicle Screw System	912-5140	FDA UDI	Class II	Active
Monaco Pedicle Screw System	902-5140	FDA UDI	Class II	Active
Brickyard Stand-Alone ALIF	SL32242014	FDA UDI	Class II	Active
Monza Cervical Plate System	135-4016	FDA UDI	Class II	Active
Valencia Pedicle Screw System	975-6530	FDA UDI	Class II	Active
Suzuka Interbody Fusion System	S410008	FDA UDI	Class II	Active
Monza Cervical Plate System	116-0483	FDA UDI	Class II	Active
Brickyard	1030-2517	FDA UDI	Class I	Active
Brickyard ALIF	FA42301215	FDA UDI	Class II	Active
Indy	1030-32241214	FDA UDI	Class II	Active
Valencia Pedicle Screw System	993-7550	FDA UDI	Class II	Active
Valencia Pedicle Screw System	973-8570	FDA UDI	Class II	Active
Fuji Cervical Plate System	122-4318	FDA UDI	Class II	Active
Monza Cervical Plate System	116-0247	FDA UDI	Class II	Active
Monza Cervical Plate System	135-4013	FDA UDI	Class II	Active
Brickyard	1030-42300812	FDA UDI	Class II	Active
Monaco Uni-Planar	813-7560	FDA UDI	Class II	Active
Indy	1020-38270818	FDA UDI	Class II	Active
Imola Interbody Fusion System	F03050-12	FDA UDI	Class II	Active
Brickyard ALIF	FA42300814	FDA UDI	Class II	Active
Valencia Pedicle Screw System	960-4525	FDA UDI	Class II	Unknown
Silverstone Titanium Interbody Fusion System	ST03206T2	FDA UDI	Class II	Active
Silverstone Interbody Fusion System	SP221007	FDA UDI	Class II	Active
Valencia Pedicle Screw System	940-7530	FDA UDI	Class II	Active
Imola Titanium Interbody Fusion System	F03045-08T	FDA UDI	Class II	Active
Brickyard ALIF	FA34261620	FDA UDI	Class II	Active
Suzuka Interbody Fusion System	ALR810	FDA UDI	Class II	Active
Sochi	A16-18-0105	FDA UDI	Class II	Active
Brickyard	1020-32240812	FDA UDI	Class II	Active
Brickyard Stand-Alone ALIF	SL38272013T	FDA UDI	Class II	Active
Fuji Cervical Plate System	100-2028	FDA UDI	Class II	Active
Monaco Pedicle Screw System	931-6120	FDA UDI	Class II	Active
Monaco Pedicle Screw System	922-5120	FDA UDI	Class II	Active
PEEK Interbody Fusion System	PL009	FDA UDI	Class II	Active
Brickyard Stand-Alone ALIF	SL38272013	FDA UDI	Class II	Active
Brickyard ALIF	FA32241619T	FDA UDI	Class II	Active
Brickyard	1020-38271612	FDA UDI	Class II	Active
Indy Standalone	SL42301613	FDA UDI	Class II	Active
Brickyard	1020-38272015	FDA UDI	Class II	Active
Monza Cervical Plate System	135-4012	FDA UDI	Class II	Active
Silverstone Titanium Interbody Fusion System	ST53209T	FDA UDI	Class II	Active

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