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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: —
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PRRC Contact: —
EUDAMED SRN: —
FDA FEI Number: —
DUNS Number: —

Catalogue (5998)

Page 16 of 120

Device	Model / Reference	Registries	Class	Status
Sochi	A16-12-4045	FDA UDI	Class II	Active
Silverstone Interbody Fusion System	PS-221016	FDA UDI	Class II	Active
Brickyard Stand-Alone ALIF	SL38272515	FDA UDI	Class II	Active
Imola Titanium Interbody Fusion System	F02640-10T	FDA UDI	Class II	Active
Fuji Cervical Plate System	112-4022	FDA UDI	Class II	Active
Fuji Cervical Plate System	137-4314	FDA UDI	Class II	Active
Monaco Pedicle Screw System	931-6155	FDA UDI	Class II	Active
Valencia Pedicle Screw System	913-5200	FDA UDI	Class II	Active
Valencia Pedicle Screw System	975-4540	FDA UDI	Class II	Active
Valencia Pedicle Screw System	975-5570	FDA UDI	Class II	Active
Brickyard	1030-42302518	FDA UDI	Class II	Active
Indy	1030-42302015	FDA UDI	Class II	Active
Suzuka Interbody Fusion System	S420010T	FDA UDI	Class II	Active
Indy Standalone	SL32242515T	FDA UDI	Class II	Active
Monaco Pedicle Screw System	822-7535	FDA UDI	Class II	Active
Imola Interbody Fusion System	F02245-08	FDA UDI	Class II	Active
Valencia Pedicle Screw System	970-7570	FDA UDI	Class II	Active
Valencia Pedicle Screw System	980-6525	FDA UDI	Class II	Active
Monaco Pedicle Screw System	922-5070	FDA UDI	Class II	Active
Imola Interbody Fusion System	F61860-08	FDA UDI	Class II	Active
Monaco Uni-Planar	813-6620	FDA UDI	Class II	Active
Indy	1020-38270809	FDA UDI	Class II	Active
Valencia Pedicle Screw System	900-1000	FDA UDI	Class II	Active
Indy Standalone	SL38271220T	FDA UDI	Class II	Active
PSS Pedicle Screw System	900-1019	FDA UDI	Class II	Unknown
Monaco Pedicle Screw System	902-5200	FDA UDI	Class II	Active
Imola Titanium Interbody Fusion System	F13055-10T	FDA UDI	Class II	Active
Indy	FA38270813T	FDA UDI	Class II	Active
Indy	FA38270812	FDA UDI	Class II	Active
Altus Spine Pedicle Screw System	880-1065	FDA UDI	Class II	Active
Suzuka Interbody Fusion System	S410509	FDA UDI	Class II	Active
Valencia Pedicle Screw System	993-8545	FDA UDI	Class II	Active
Brickyard	1020-34260819	FDA UDI	Class II	Active
Sochi	A10-24-1420	FDA UDI	Class II	Active
Silverstone Interbody Fusion System	SP261009	FDA UDI	Class II	Active
Valencia Pedicle Screw System	960-5545	FDA UDI	Class II	Unknown
Indy	FA38272018	FDA UDI	Class II	Active
Altus Spine Pedicle Screw System	981-0004TN	FDA UDI	Class II	Active
Altus Spine Interbody Fusion System	1001-2616	FDA UDI	Class II	Active
Valencia Pedicle Screw System	993-7570	FDA UDI	Class II	Active
Fuji Cervical Plate System	114-0250	FDA UDI	Class II	Active
Brickyard ALIF	FA32242014	FDA UDI	Class II	Active
Valencia Pedicle Screw System	930-5535	FDA UDI	Class II	Active
Imola-Silverstone	700-1040	FDA UDI	Class II	Active
Brickyard ALIF	FA42300818	FDA UDI	Class II	Active
Silverstone Titanium Interbody Fusion System	ST82810T	FDA UDI	Class II	Active
Indy	FA34261213	FDA UDI	Class II	Active
Sochi	A16-23-5550	FDA UDI	Class II	Active
Indy Standalone	SL38271218	FDA UDI	Class II	Active
Indy	FA34261215T	FDA UDI	Class II	Active

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