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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 37 of 120

Device	Model / Reference	Registries	Class	Status
Indy Standalone	SL42300815	FDA UDI	Class II	Active
Brickyard ALIF	FA32241220	FDA UDI	Class II	Active
Monaco Pedicle Screw System	921-6045	FDA UDI	Class II	Active
Brickyard Stand-Alone ALIF	1030-0900	FDA UDI	Class I	Active
Imola Interbody Fusion System	F11840-14	FDA UDI	Class II	Active
Valencia Pedicle Screw System	993-7540	FDA UDI	Class II	Active
Monza Cervical Plate System	116-0253	FDA UDI	Class II	Active
Silverstone Interbody Fusion System	PS-301018	FDA UDI	Class II	Active
Brickyard ALIF	FA34262013T	FDA UDI	Class II	Active
Brickyard Stand-Alone ALIF	SL38272515T	FDA UDI	Class II	Active
Brickyard Stand-Alone ALIF	SL32242518T	FDA UDI	Class II	Active
Indy	1020-34260814	FDA UDI	Class II	Active
Indy Standalone	SL32242520T	FDA UDI	Class II	Active
Valencia Pedicle Screw System	983-6530	FDA UDI	Class II	Active
Monaco Pedicle Screw System	911-5050	FDA UDI	Class II	Active
Brickyard	1030-38270814	FDA UDI	Class II	Active
Brickyard Stand-Alone ALIF	SL0013	FDA UDI	Class II	Active
Altus Spine Pedicle Screw System	905-0057	FDA UDI	Class II	Active
Monaco Pedicle Screw System	921-6040	FDA UDI	Class II	Active
Brickyard Stand-Alone ALIF	SL32241617	FDA UDI	Class II	Active
Monaco Uni-Planar	811-5045	FDA UDI	Class II	Active
Valencia Pedicle Screw System	970-6555	FDA UDI	Class II	Active
Valencia Pedicle Screw System	990-7540	FDA UDI	Class II	Active
Indy	FA42300811	FDA UDI	Class II	Active
Monaco Pedicle Screw System	922-5145	FDA UDI	Class II	Active
Imola Titanium Interbody Fusion System	F11845-14T	FDA UDI	Class II	Active
Monaco Pedicle Screw System	811-9530	FDA UDI	Class II	Active
Brickyard	1030-38271618	FDA UDI	Class II	Active
Valencia Pedicle Screw System	930-7530	FDA UDI	Class II	Active
Imola Titanium Interbody Fusion System	F01845-16T	FDA UDI	Class II	Active
Valencia Pedicle Screw System	922-5530	FDA UDI	Class II	Unknown
Valencia Pedicle Screw System	990-5525	FDA UDI	Class II	Active
Brickyard ALIF	FA32241620T	FDA UDI	Class II	Active
Valencia Pedicle Screw System	993-8595	FDA UDI	Class II	Active
Monaco Pedicle Screw System	811-6525	FDA UDI	Class II	Active
Monaco Pedicle Screw System	822-9590	FDA UDI	Class II	Active
Brickyard Stand-Alone ALIF	SL42301616	FDA UDI	Class II	Active
Valencia Pedicle Screw System	950-5525	FDA UDI	Class II	Active
Brickyard ALIF	FA38270815T	FDA UDI	Class II	Active
Valencia Pedicle Screw System	993-8530	FDA UDI	Class II	Active
Monza Cervical Plate System	120-4312	FDA UDI	Class II	Active
Monaco Pedicle Screw System	901-6060	FDA UDI	Class II	Active
Altus Spine Interbody Fusion System	1000-2208	FDA UDI	Class II	Active
Silverstone Titanium Interbody Fusion System	SP301017T	FDA UDI	Class II	Active
Silverstone Titanium Interbody Fusion System	ST83206T	FDA UDI	Class II	Active
Valencia Pedicle Screw System	993-7525	FDA UDI	Class II	Active
Silverstone Interbody Fusion System	SP261010	FDA UDI	Class II	Active
Indy	1020-38270817	FDA UDI	Class II	Active
Indy	1020-100H	FDA UDI	Class I	Active
Altus Spine Interbody Fusion System	1000-2212L	FDA UDI	Class II	Active

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