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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: —
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Phone: —
PRRC Contact: —
EUDAMED SRN: —
FDA FEI Number: —
DUNS Number: —

Catalogue (5998)

Page 21 of 120

Device	Model / Reference	Registries	Class	Status
Indy	1030-1613	FDA UDI	Class I	Active
Valencia Pedicle Screw System	980-7590	FDA UDI	Class II	Active
Imola Interbody Fusion System	F01855-16	FDA UDI	Class II	Active
Silverstone Interbody Fusion System	SP301008	FDA UDI	Class II	Active
Silverstone Titanium Interbody Fusion System	ST03215T2	FDA UDI	Class II	Active
Valencia Pedicle Screw System	930-6525	FDA UDI	Class II	Active
Imola Titanium Interbody Fusion System	F12650-10T	FDA UDI	Class II	Active
Indy	FA42301617	FDA UDI	Class II	Active
Imola Titanium Interbody Fusion System	F12655-12T	FDA UDI	Class II	Active
Imola Titanium Interbody Fusion System	F12645-14T	FDA UDI	Class II	Active
Altus Spine HA Pedicle Screw System	811-8590HA	FDA UDI	Class II	Active
Brickyard ALIF	FA34260809	FDA UDI	Class II	Active
Monaco Uni-Planar	813-6525	FDA UDI	Class II	Active
Brickyard ALIF	FA34261211	FDA UDI	Class II	Active
Sochi	A10-23-0120	FDA UDI	Class II	Active
Suzuka Interbody Fusion System	ALR110	FDA UDI	Class II	Active
Monza Cervical Plate System	116-0474	FDA UDI	Class II	Active
Valencia Pedicle Screw System	990-5545	FDA UDI	Class II	Active
Monaco Pedicle Screw System	911-6080	FDA UDI	Class II	Active
Valencia Pedicle Screw System	930-8545	FDA UDI	Class II	Active
Indy Standalone	SLV4235	FDA UDI	Class II	Active
Indy Standalone	SL32241614T	FDA UDI	Class II	Active
Indy	FA42300811T	FDA UDI	Class II	Active
Imola-Silverstone	700-0022	FDA UDI	Class II	Active
Monaco Pedicle Screw System	921-6130	FDA UDI	Class II	Active
Imola Titanium Interbody Fusion System	F02645-12T	FDA UDI	Class II	Active
Imola Titanium Interbody Fusion System	F61845-08T	FDA UDI	Class II	Active
Altus Spine Interbody Fusion System	1000-2216	FDA UDI	Class II	Active
Suzuka Interbody Fusion System	ALR029	FDA UDI	Class II	Active
Altus Spine Interbody Fusion System	722-2014	FDA UDI	Class II	Active
Monza Cervical Plate System	100-1003	FDA UDI	Class II	Active
Altus Spine Interbody Fusion System	1001-3016	FDA UDI	Class II	Active
Indy	FA42301219	FDA UDI	Class II	Active
Brickyard	1030-32242518	FDA UDI	Class II	Active
Imola Interbody Fusion System	F02260-12	FDA UDI	Class II	Active
Altus Spine Interbody Fusion System	1001-3014	FDA UDI	Class II	Active
Altus Spine Interbody Fusion System	790-0013	FDA UDI	Class II	Active
Monaco Pedicle Screw System	932-5040	FDA UDI	Class II	Active
Monaco Pedicle Screw System	822-8555	FDA UDI	Class II	Active
Monaco Pedicle Screw System	811-8570	FDA UDI	Class II	Active
Altus Spine HA Pedicle Screw System	811-6050HA	FDA UDI	Class II	Active
Fuji Cervical Plate System	138-4022	FDA UDI	Class II	Active
Monaco Pedicle Screw System	822-8530	FDA UDI	Class II	Active
Imola Interbody Fusion System	F12650-16	FDA UDI	Class II	Active
Sochi	A16-18-1090	FDA UDI	Class II	Active
Monza Cervical Plate System	135-4018	FDA UDI	Class II	Active
Valencia Pedicle Screw System	943-6540	FDA UDI	Class II	Active
Monza Cervical Plate System	116-0353	FDA UDI	Class II	Active
Indy	1030-38270820	FDA UDI	Class II	Active
Indy	1030-1216	FDA UDI	Class I	Active

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