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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 34 of 120

Device	Model / Reference	Registries	Class	Status
Brickyard	1020-34262515	FDA UDI	Class II	Active
Fuji Cervical Plate System	121-4018	FDA UDI	Class II	Active
Brickyard ALIF	FA34262518	FDA UDI	Class II	Active
Brickyard Stand-Alone ALIF	1030-2415A	FDA UDI	Class I	Active
Altus Spine Interbody Fusion System	790-0008	FDA UDI	Class II	Active
Monaco Uni-Planar	813-6545	FDA UDI	Class II	Active
Indy	1020-32241210	FDA UDI	Class II	Active
Indy	FA34261615	FDA UDI	Class II	Active
Indy Standalone	SL42300812	FDA UDI	Class II	Active
Imola Interbody Fusion System	F01840-16	FDA UDI	Class II	Active
Imola Interbody Fusion System	F02645-10	FDA UDI	Class II	Active
Imola-Silverstone	707-1017	FDA UDI	Class II	Active
Imola Interbody Fusion System	FA082634-14	FDA UDI	Class II	Active
Valencia Pedicle Screw System	990-8540	FDA UDI	Class II	Active
Sochi	A16-18-0090	FDA UDI	Class II	Active
Imola Interbody Fusion System	F02255-08	FDA UDI	Class II	Active
Brickyard	1030-38270817	FDA UDI	Class II	Active
Indy Standalone	1030-2415A	FDA UDI	Class I	Active
Fuji Cervical Plate System	114-0371	FDA UDI	Class II	Active
Valencia Pedicle Screw System	922-7550	FDA UDI	Class II	Unknown
Imola Interbody Fusion System	F11845-16	FDA UDI	Class II	Active
Imola Interbody Fusion System	F12645-14	FDA UDI	Class II	Active
Valencia Pedicle Screw System	930-8530	FDA UDI	Class II	Active
Monaco Uni-Planar	813-9530	FDA UDI	Class II	Active
Sochi	A16-18-0200	FDA UDI	Class II	Active
Indy Standalone	SL42300816	FDA UDI	Class II	Active
Altus Spine HA Pedicle Screw System	811-5050HA	FDA UDI	Class II	Active
Silverstone Titanium Interbody Fusion System	ST53207T	FDA UDI	Class II	Active
Sochi	A16-30-3848	FDA UDI	Class II	Active
Altus Spine Cervical Interbody Fusion System	245-0004	FDA UDI	Class II	Active
Altus Spine Interbody Fusion System	1000-1808	FDA UDI	Class II	Active
Fuji Cervical Plate System	136-4018	FDA UDI	Class II	Active
Monaco Pedicle Screw System	911-5160	FDA UDI	Class II	Active
Suzuka Interbody Fusion System	S411007	FDA UDI	Class II	Active
Silverstone Titanium Interbody Fusion System	ST03211T	FDA UDI	Class II	Active
Silverstone Titanium Interbody Fusion System	ST82206T	FDA UDI	Class II	Active
Silverstone Titanium Interbody Fusion System	ST82207T	FDA UDI	Class II	Active
Brickyard Stand-Alone ALIF	SL42301616T	FDA UDI	Class II	Active
Indy Standalone	SL32242012T	FDA UDI	Class II	Active
Suzuka Interbody Fusion System	S410508	FDA UDI	Class II	Active
Brickyard ALIF	FA42302518	FDA UDI	Class II	Active
Suzuka Interbody Fusion System	ALR026	FDA UDI	Class II	Active
Imola Titanium Interbody Fusion System	F02255-10T	FDA UDI	Class II	Active
Imola Titanium Interbody Fusion System	F12650-12T	FDA UDI	Class II	Active
Monaco Pedicle Screw System	822-9540	FDA UDI	Class II	Active
Valencia Pedicle Screw System	924-5610	FDA UDI	Class II	Active
Indy	FA42300817T	FDA UDI	Class II	Active
Monaco Pedicle Screw System	811-4560	FDA UDI	Class II	Active
Altus Spine Pedicle Screw System	905-0046	FDA UDI	Class II	Active
Suzuka Interbody Fusion System	S730805T	FDA UDI	Class II	Active

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