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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 92 of 120

Device	Model / Reference	Registries	Class	Status
Monaco Pedicle Screw System	911-5180	FDA UDI	Class II	Active
Indy Standalone	1030-2135A	FDA UDI	Class I	Active
Brickyard ALIF	FA42300819T	FDA UDI	Class II	Active
Indy	1030-42301216	FDA UDI	Class II	Active
Valencia Pedicle Screw System	943-7545	FDA UDI	Class II	Active
Indy Standalone	SL38272018T	FDA UDI	Class II	Active
Valencia Pedicle Screw System	993-7590	FDA UDI	Class II	Active
Brickyard ALIF	FA32242016	FDA UDI	Class II	Active
Altus Spine Pedicle Screw System	908-0058	FDA UDI	Class II	Active
Valencia Pedicle Screw System	930-5560	FDA UDI	Class II	Active
Suzuka Interbody Fusion System	ALR031	FDA UDI	Class II	Active
Valencia Pedicle Screw System	960-8550	FDA UDI	Class II	Unknown
Suzuka Interbody Fusion System	ALR508	FDA UDI	Class II	Active
Sochi	A16-23-3510	FDA UDI	Class II	Active
Silverstone Titanium Interbody Fusion System	ST83208T	FDA UDI	Class II	Active
Imola Titanium Interbody Fusion System	F12255-16T	FDA UDI	Class II	Active
Valencia Pedicle Screw System	925-6545	FDA UDI	Class II	Unknown
Indy	1030-38271214	FDA UDI	Class II	Active
Indy	1020-32240808	FDA UDI	Class II	Active
Indy	FA34262020T	FDA UDI	Class II	Active
Suzuka Interbody Fusion System	S410510T	FDA UDI	Class II	Active
Monaco Uni-Planar	813-7550	FDA UDI	Class II	Active
Indy Standalone	1030-0125A	FDA UDI	Class I	Active
Monaco Pedicle Screw System	811-5525	FDA UDI	Class II	Active
Valencia Pedicle Screw System	922-5555	FDA UDI	Class II	Unknown
Valencia Pedicle Screw System	925-5550	FDA UDI	Class II	Unknown
Indy	1020-38272019	FDA UDI	Class II	Active
Altus Spine HA Pedicle Screw System	822-9600HA	FDA UDI	Class II	Active
Fuji Cervical Plate System	136-4012	FDA UDI	Class II	Active
Indy	1020-42300813	FDA UDI	Class II	Active
Fuji Cervical Plate System	114-0368	FDA UDI	Class II	Active
Imola Interbody Fusion System	F11855-16	FDA UDI	Class II	Active
Altus Spine Cervical Interbody Fusion System	210-3005	FDA UDI	Class II	Active
Indy	1030-42302518	FDA UDI	Class II	Active
Imola Interbody Fusion System	F02655-10	FDA UDI	Class II	Active
Imola Titanium Interbody Fusion System	F02245-08T	FDA UDI	Class II	Active
Valencia Pedicle Screw System	970-8575	FDA UDI	Class II	Active
Indy Standalone	1030-4225G-45	FDA UDI	Class II	Active
Silverstone Titanium Interbody Fusion System	ST83213T2	FDA UDI	Class II	Active
Brickyard ALIF	FA34261219	FDA UDI	Class II	Active
Indy Standalone	SL38271617	FDA UDI	Class II	Active
Brickyard ALIF	FA34260809T	FDA UDI	Class II	Active
Monaco Uni-Planar	813-6535	FDA UDI	Class II	Active
Brickyard	1030-0811	FDA UDI	Class I	Active
Monaco Uni-Planar	813-5525	FDA UDI	Class II	Active
Indy	FA38270817	FDA UDI	Class II	Active
Brickyard	1030-42301618	FDA UDI	Class II	Active
Valencia Pedicle Screw System	990-6540	FDA UDI	Class II	Active
Indy Standalone	SL32241213T	FDA UDI	Class II	Active
Valencia Pedicle Screw System	993-8550	FDA UDI	Class II	Active

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