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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 95 of 120

Device	Model / Reference	Registries	Class	Status
Valencia Pedicle Screw System	940-5525	FDA UDI	Class II	Active
Valencia Pedicle Screw System	923-5155	FDA UDI	Class II	Active
Valencia Pedicle Screw System	950-5560	FDA UDI	Class II	Active
Brickyard ALIF	FA34261217	FDA UDI	Class II	Active
Brickyard	1030-1112	FDA UDI	Class I	Active
Imola Titanium Interbody Fusion System	F03060-10T	FDA UDI	Class II	Active
Suzuka Interbody Fusion System	S420807	FDA UDI	Class II	Active
Indy	1020-34260816	FDA UDI	Class II	Active
Indy Standalone	1030-0100A	FDA UDI	Class I	Active
Valencia Pedicle Screw System	905-1011	FDA UDI	Class II	Active
Brickyard	1020-34262013	FDA UDI	Class II	Active
Brickyard Stand-Alone ALIF	1030-0235	FDA UDI	Class II	Active
Silverstone Titanium Interbody Fusion System	ST82215T	FDA UDI	Class II	Active
Imola Titanium Interbody Fusion System	F13040-14T	FDA UDI	Class II	Active
Brickyard ALIF	FA34260810	FDA UDI	Class II	Active
Silverstone Titanium Interbody Fusion System	ST52210T2	FDA UDI	Class II	Active
Imola Titanium Interbody Fusion System	F03040-16T	FDA UDI	Class II	Active
Brickyard	1030-1117	FDA UDI	Class I	Active
Monaco Pedicle Screw System	931-6090	FDA UDI	Class II	Active
Indy Standalone	SL42301619T	FDA UDI	Class II	Active
Indy	FA42302016	FDA UDI	Class II	Active
Silverstone Titanium Interbody Fusion System	ST52808	FDA UDI	Class II	Active
Indy	FA42300813	FDA UDI	Class II	Active
Altus Spine HA Pedicle Screw System	811-5525HA	FDA UDI	Class II	Active
Silverstone Titanium Interbody Fusion System	ST52809T	FDA UDI	Class II	Active
Indy	FA32240817T	FDA UDI	Class II	Active
Valencia Pedicle Screw System	975-6560	FDA UDI	Class II	Active
Silverstone Titanium Interbody Fusion System	ST82807T	FDA UDI	Class II	Active
Valencia Pedicle Screw System	942-8550	FDA UDI	Class II	Unknown
Suzuka Interbody Fusion System	S410010T	FDA UDI	Class II	Active
Sochi	A16-12-5016	FDA UDI	Class II	Active
Imola-Silverstone	705-3015	FDA UDI	Class II	Active
Brickyard ALIF	FA32242012T	FDA UDI	Class II	Active
Altus Spine Pedicle Screw System	908-0033	FDA UDI	Class II	Active
Silverstone Titanium Interbody Fusion System	ST03213T	FDA UDI	Class II	Active
Brickyard ALIF	FA34261614	FDA UDI	Class II	Active
Monaco Pedicle Screw System	902-6050	FDA UDI	Class II	Active
Silverstone Titanium Interbody Fusion System	ST02811T2	FDA UDI	Class II	Active
Valencia Pedicle Screw System	970-5530	FDA UDI	Class II	Active
Altus Spine Interbody Fusion System	722-2009	FDA UDI	Class II	Active
Suzuka Interbody Fusion System	S410511T	FDA UDI	Class II	Active
Suzuka Interbody Fusion System	ALR511	FDA UDI	Class II	Active
Valencia Pedicle Screw System	960-4560	FDA UDI	Class II	Unknown
Altus Spine Pedicle Screw System	908-1033TN	FDA UDI	Class II	Active
Silverstone Interbody Fusion System	SEC00928-13	FDA UDI	Class II	Active
Brickyard ALIF	FA32241620	FDA UDI	Class II	Active
Imola Titanium Interbody Fusion System	F12260-12T	FDA UDI	Class II	Active
Altus Spine HA Pedicle Screw System	822-7600HA	FDA UDI	Class II	Active
Brickyard	1020-42301616	FDA UDI	Class II	Active
Brickyard	1020-0042	FDA UDI	Class I	Active

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