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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 41 of 120

Device	Model / Reference	Registries	Class	Status
PEEK Interbody Fusion System	PL512	FDA UDI	Class II	Active
Silverstone Titanium Interbody Fusion System	SP261016T2	FDA UDI	Class II	Active
Imola Titanium Interbody Fusion System	F12660-12T	FDA UDI	Class II	Active
Sochi	A16-12-4510	FDA UDI	Class II	Active
Altus Spine HA Pedicle Screw System	811-6555HA	FDA UDI	Class II	Active
Monaco Pedicle Screw System	902-5070	FDA UDI	Class II	Active
Suzuka Interbody Fusion System	S730009T	FDA UDI	Class II	Active
Indy Standalone	1030-0100G-45	FDA UDI	Class II	Active
Monaco Pedicle Screw System	822-6555	FDA UDI	Class II	Active
Valencia Pedicle Screw System	913-5095	FDA UDI	Class II	Active
Imola Interbody Fusion System	F12655-10	FDA UDI	Class II	Active
Brickyard	1030-38272015	FDA UDI	Class II	Active
Monaco Uni-Planar	813-8590	FDA UDI	Class II	Active
Suzuka Interbody Fusion System	ALR17-110	FDA UDI	Class II	Active
Monaco Uni-Planar	880-6311C	FDA UDI	Class II	Active
Altus Spine HA Pedicle Screw System	822-9540HA	FDA UDI	Class II	Active
Imola Titanium Interbody Fusion System	F02655-12T	FDA UDI	Class II	Active
Monaco Uni-Planar	813-7535	FDA UDI	Class II	Active
Brickyard	1030-32241618	FDA UDI	Class II	Active
Brickyard ALIF	FA32241213T	FDA UDI	Class II	Active
Altus Spine HA Pedicle Screw System	811-4540HA	FDA UDI	Class II	Active
Imola Interbody Fusion System	F03040-08	FDA UDI	Class II	Active
Monza Cervical Plate System	116-0377	FDA UDI	Class II	Active
Imola Titanium Interbody Fusion System	F02240-10T	FDA UDI	Class II	Active
Valencia Pedicle Screw System	943-6550	FDA UDI	Class II	Active
Imola Titanium Interbody Fusion System	F02660-16T	FDA UDI	Class II	Active
Brickyard	1030-1119	FDA UDI	Class I	Active
Indy Standalone	SL38271620T	FDA UDI	Class II	Active
Indy	1020-38270814	FDA UDI	Class II	Active
Indy Standalone	1030-4225	FDA UDI	Class II	Active
Monaco Pedicle Screw System	931-6180	FDA UDI	Class II	Active
Valencia Pedicle Screw System	900-1023	FDA UDI	Class II	Unknown
Monaco Pedicle Screw System	922-6110	FDA UDI	Class II	Active
Brickyard Stand-Alone ALIF	1030-0016	FDA UDI	Class II	Active
Indy	FA38272019	FDA UDI	Class II	Active
Monaco Pedicle Screw System	902-5040	FDA UDI	Class II	Active
Imola Titanium Interbody Fusion System	F02255-14T	FDA UDI	Class II	Active
Brickyard Stand-Alone ALIF	1030-2440A	FDA UDI	Class I	Active
Sochi	A16-12-4525	FDA UDI	Class II	Active
Indy	FA38270810T	FDA UDI	Class II	Active
Monaco Uni-Planar	811-5035	FDA UDI	Class II	Active
Suzuka Interbody Fusion System	ALR529	FDA UDI	Class II	Active
Monaco Pedicle Screw System	901-6100	FDA UDI	Class II	Active
Valencia Pedicle Screw System	975-5550	FDA UDI	Class II	Active
Valencia Pedicle Screw System	922-4540	FDA UDI	Class II	Unknown
Silverstone Titanium Interbody Fusion System	ST52814T2	FDA UDI	Class II	Active
Monaco Pedicle Screw System	901-5200	FDA UDI	Class II	Active
PEEK Interbody Fusion System	PL011	FDA UDI	Class II	Active
Brickyard ALIF	FA34261212T	FDA UDI	Class II	Active
Brickyard ALIF	FA38271217T	FDA UDI	Class II	Active

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