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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 17 of 120

Device	Model / Reference	Registries	Class	Status
Silverstone Titanium Interbody Fusion System	ST82216T	FDA UDI	Class II	Active
Valencia Pedicle Screw System	924-5645	FDA UDI	Class II	Active
Altus Spine Pedicle Screw System	975-0006	FDA UDI	Class II	Active
Indy Standalone	SL42301218T	FDA UDI	Class II	Active
Brickyard Stand-Alone ALIF	SL32241214T	FDA UDI	Class II	Active
Monza Cervical Plate System	135-4014	FDA UDI	Class II	Active
Valencia Pedicle Screw System	940-7580	FDA UDI	Class II	Active
Valencia Pedicle Screw System	960-5530	FDA UDI	Class II	Unknown
Valencia Pedicle Screw System	923-5085	FDA UDI	Class II	Active
Monaco Uni-Planar	813-9580	FDA UDI	Class II	Active
Monaco Pedicle Screw System	932-5150	FDA UDI	Class II	Active
Brickyard Stand-Alone ALIF	SL42302517T	FDA UDI	Class II	Active
Imola Interbody Fusion System	FA152634-14	FDA UDI	Class II	Active
Valencia Pedicle Screw System	922-4530	FDA UDI	Class II	Unknown
Monaco Pedicle Screw System	822-8610	FDA UDI	Class II	Active
Monza Cervical Plate System	116-0374	FDA UDI	Class II	Active
Valencia Pedicle Screw System	973-8565	FDA UDI	Class II	Active
Imola Interbody Fusion System	F01840-08	FDA UDI	Class II	Active
Suzuka Interbody Fusion System	S420806	FDA UDI	Class II	Active
Indy	1030-32242019	FDA UDI	Class II	Active
Monaco Pedicle Screw System	822-9560	FDA UDI	Class II	Active
Monaco Pedicle Screw System	811-7590	FDA UDI	Class II	Active
Brickyard Stand-Alone ALIF	SL42302519T	FDA UDI	Class II	Active
Silverstone Interbody Fusion System	SEC00932-14	FDA UDI	Class II	Active
Brickyard Stand-Alone ALIF	SL42302020	FDA UDI	Class II	Active
Altus Spine HA Pedicle Screw System	811-5540HA	FDA UDI	Class II	Active
Valencia Pedicle Screw System	993-8555	FDA UDI	Class II	Active
Fuji Cervical Plate System	114-0347	FDA UDI	Class II	Active
Imola Interbody Fusion System	F03060-16	FDA UDI	Class II	Active
Sochi	A16-12-5028	FDA UDI	Class II	Active
Altus Spine HA Pedicle Screw System	811-9530HA	FDA UDI	Class II	Active
Indy	FA32242019T	FDA UDI	Class II	Active
Suzuka Interbody Fusion System	ALR17-507	FDA UDI	Class II	Active
Indy Standalone	SL38271216T	FDA UDI	Class II	Active
Indy	FA38270816	FDA UDI	Class II	Active
Altus Spine Interbody Fusion System	722-2011	FDA UDI	Class II	Active
Imola Titanium Interbody Fusion System	F11860-14T	FDA UDI	Class II	Active
Sochi	A16-10-3512	FDA UDI	Class II	Active
Brickyard ALIF	FA34261612T	FDA UDI	Class II	Active
Imola-Silverstone	707-1008	FDA UDI	Class II	Active
Altus Spine Pedicle Screw System	880-1045	FDA UDI	Class II	Active
Altus Spine Pedicle Screw System	900-1029	FDA UDI	Class II	Active
Indy	1020-38270813	FDA UDI	Class II	Active
Indy	FA42302018T	FDA UDI	Class II	Active
Monaco Pedicle Screw System	912-5090	FDA UDI	Class II	Active
Indy	1030-32241213	FDA UDI	Class II	Active
Brickyard ALIF	FA32241614T	FDA UDI	Class II	Active
Monaco Pedicle Screw System	912-5080	FDA UDI	Class II	Active
Indy	1030-1209	FDA UDI	Class I	Active
Valencia Pedicle Screw System	930-7525	FDA UDI	Class II	Active

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