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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 106 of 120

Device	Model / Reference	Registries	Class	Status
Brickyard Stand-Alone ALIF	SL42302520T	FDA UDI	Class II	Active
Imola Interbody Fusion System	F12260-14	FDA UDI	Class II	Active
Valencia Pedicle Screw System	940-7535	FDA UDI	Class II	Active
Indy	1020-38271220	FDA UDI	Class II	Active
Silverstone Titanium Interbody Fusion System	ST52212T2	FDA UDI	Class II	Active
PEEK Interbody Fusion System	PL509	FDA UDI	Class II	Active
Valencia Pedicle Screw System	950-8545	FDA UDI	Class II	Active
Monaco Pedicle Screw System	922-6115	FDA UDI	Class II	Active
Valencia Pedicle Screw System	925-4560	FDA UDI	Class II	Unknown
Valencia Pedicle Screw System	943-7600	FDA UDI	Class II	Active
Valencia Pedicle Screw System	960-8560	FDA UDI	Class II	Unknown
PEEK Interbody Fusion System	TL009	FDA UDI	Class II	Active
Imola Titanium Interbody Fusion System	F13055-14T	FDA UDI	Class II	Active
Imola Titanium Interbody Fusion System	F12255-12T	FDA UDI	Class II	Active
Indy Standalone	SL38272516	FDA UDI	Class II	Active
Monaco Pedicle Screw System	822-6545	FDA UDI	Class II	Active
Monaco Uni-Planar	813-6530	FDA UDI	Class II	Active
Brickyard Stand-Alone ALIF	1030-2045	FDA UDI	Class I	Active
Brickyard Stand-Alone ALIF	SL38272014T	FDA UDI	Class II	Active
Valencia Pedicle Screw System	940-6540	FDA UDI	Class II	Active
Sochi	A16-32-4514	FDA UDI	Class II	Active
Silverstone Titanium Interbody Fusion System	ST52209T	FDA UDI	Class II	Active
Brickyard	1020-42301617	FDA UDI	Class II	Active
Brickyard ALIF	1020-1215	FDA UDI	Class II	Active
Brickyard ALIF	FA34261220	FDA UDI	Class II	Active
Monaco Pedicle Screw System	922-5085	FDA UDI	Class II	Active
Valencia Pedicle Screw System	980-7585	FDA UDI	Class II	Active
Sochi	A16-32-4515	FDA UDI	Class II	Active
Monaco Pedicle Screw System	932-6155	FDA UDI	Class II	Active
Suzuka Interbody Fusion System	S730811	FDA UDI	Class II	Active
Monaco Pedicle Screw System	921-6090	FDA UDI	Class II	Active
Brickyard	1030-32242015	FDA UDI	Class II	Active
Indy Standalone	SL38272014	FDA UDI	Class II	Active
Indy	1030-38270812	FDA UDI	Class II	Active
Silverstone Titanium Interbody Fusion System	ST02211T2	FDA UDI	Class II	Active
Brickyard Stand-Alone ALIF	1030-4235	FDA UDI	Class II	Active
Silverstone Interbody Fusion System	PS-261010	FDA UDI	Class II	Active
Brickyard Stand-Alone ALIF	SL38271214	FDA UDI	Class II	Active
Brickyard	1020-32241216	FDA UDI	Class II	Active
Monaco Uni-Planar	831-1702	FDA UDI	Class II	Active
Monza Cervical Plate System	116-0130	FDA UDI	Class II	Active
Imola Interbody Fusion System	F02640-08	FDA UDI	Class II	Active
Fuji Cervical Plate System	114-0241	FDA UDI	Class II	Active
Indy Standalone	SL38271619	FDA UDI	Class II	Active
Imola Interbody Fusion System	F61845-08	FDA UDI	Class II	Active
Sochi	A16-18-1075	FDA UDI	Class II	Active
Indy	1030-0810	FDA UDI	Class I	Active
Valencia Pedicle Screw System	970-4535	FDA UDI	Class II	Active
Silverstone Titanium Interbody Fusion System	ST52809	FDA UDI	Class II	Active
Valencia Pedicle Screw System	990-7535	FDA UDI	Class II	Active

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