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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 86 of 120

Device	Model / Reference	Registries	Class	Status
Valencia Pedicle Screw System	940-8530	FDA UDI	Class II	Active
Monaco Pedicle Screw System	921-6100	FDA UDI	Class II	Active
Brickyard ALIF	FA32241617T	FDA UDI	Class II	Active
Monaco Pedicle Screw System	902-5060	FDA UDI	Class II	Active
Sochi	A16-12-4550	FDA UDI	Class II	Active
Silverstone Titanium Interbody Fusion System	SP221015T2	FDA UDI	Class II	Active
Altus Spine Interbody Fusion System	1001-2608	FDA UDI	Class II	Active
Monaco Pedicle Screw System	921-6120	FDA UDI	Class II	Active
Monaco Pedicle Screw System	811-4550	FDA UDI	Class II	Active
Valencia Pedicle Screw System	975-8530	FDA UDI	Class II	Active
Altus Spine Pedicle Screw System	975-0005	FDA UDI	Class II	Active
PEEK Interbody Fusion System	TL22013	FDA UDI	Class II	Active
Suzuka Interbody Fusion System	S421010T	FDA UDI	Class II	Active
Brickyard Stand-Alone ALIF	SL42302520	FDA UDI	Class II	Active
Brickyard	1020-34260809	FDA UDI	Class II	Active
Monaco Pedicle Screw System	921-6075	FDA UDI	Class II	Active
Brickyard	1020-42302019	FDA UDI	Class II	Active
Valencia Pedicle Screw System	973-5550	FDA UDI	Class II	Active
Brickyard	1030-32242514	FDA UDI	Class II	Active
Monaco Pedicle Screw System	911-6400	FDA UDI	Class II	Active
Valencia Pedicle Screw System	983-6555	FDA UDI	Class II	Active
Monaco Pedicle Screw System	931-6055	FDA UDI	Class II	Active
Imola-Silverstone	1000-0738	FDA UDI	Class II	Active
Monaco Pedicle Screw System	811-9570	FDA UDI	Class II	Active
Suzuka Interbody Fusion System	S421006	FDA UDI	Class II	Active
Sochi	A16-18-0050	FDA UDI	Class II	Active
Indy Standalone	SL32242018T	FDA UDI	Class II	Active
Indy	1020-32242016	FDA UDI	Class II	Active
Monaco Pedicle Screw System	932-6105	FDA UDI	Class II	Active
Indy	1030-32241210	FDA UDI	Class II	Active
Indy	FA34260815T	FDA UDI	Class II	Active
Valencia Pedicle Screw System	930-8550	FDA UDI	Class II	Active
Fuji Cervical Plate System	137-4316	FDA UDI	Class II	Active
Brickyard Stand-Alone ALIF	SL32241618T	FDA UDI	Class II	Active
Brickyard ALIF	FA38272015T	FDA UDI	Class II	Active
Valencia Pedicle Screw System	943-7590	FDA UDI	Class II	Active
Silverstone Titanium Interbody Fusion System	SP301010T	FDA UDI	Class II	Active
Altus Spine HA Pedicle Screw System	811-6535HA	FDA UDI	Class II	Active
Indy	FA38271215T	FDA UDI	Class II	Active
Indy	FA38271212	FDA UDI	Class II	Active
Monaco Pedicle Screw System	912-5200	FDA UDI	Class II	Active
Suzuka Interbody Fusion System	S410811T	FDA UDI	Class II	Active
Monaco Uni-Planar	813-7540	FDA UDI	Class II	Active
Indy	FA34262018T	FDA UDI	Class II	Active
Brickyard Stand-Alone ALIF	1030-0220G-45	FDA UDI	Class II	Active
Brickyard	1020-32242019	FDA UDI	Class II	Active
Brickyard	1030-42302018	FDA UDI	Class II	Active
Fuji Cervical Plate System	111-4022	FDA UDI	Class II	Active
Imola-Silverstone	705-3014	FDA UDI	Class II	Active
Valencia Pedicle Screw System	943-8540	FDA UDI	Class II	Active

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