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

Catalogue (5998)

Page 35 of 120

Device	Model / Reference	Registries	Class	Status
Altus Spine Cervical Interbody Fusion System	210-0008	FDA UDI	Class II	Active
Monaco Pedicle Screw System	921-5040	FDA UDI	Class II	Active
Imola Titanium Interbody Fusion System	F12660-16T	FDA UDI	Class II	Active
Brickyard ALIF	FA34261213	FDA UDI	Class II	Active
Sochi	A10-24-1135	FDA UDI	Class II	Active
Brickyard ALIF	FA38271215	FDA UDI	Class II	Active
Valencia Pedicle Screw System	975-7560	FDA UDI	Class II	Active
Brickyard ALIF	FA32241611T	FDA UDI	Class II	Active
Suzuka Interbody Fusion System	S410009	FDA UDI	Class II	Active
Suzuka Interbody Fusion System	S411008	FDA UDI	Class II	Active
Indy	FA42301615	FDA UDI	Class II	Active
Indy	1020-42302518	FDA UDI	Class II	Active
Monza Cervical Plate System	110-4012	FDA UDI	Class II	Active
Silverstone Interbody Fusion System	PS-301011	FDA UDI	Class II	Active
Valencia Pedicle Screw System	973-7580	FDA UDI	Class II	Active
Silverstone Interbody Fusion System	PS-301017	FDA UDI	Class II	Active
Valencia Pedicle Screw System	983-6525	FDA UDI	Class II	Active
Valencia Pedicle Screw System	975-5525	FDA UDI	Class II	Active
Valencia Pedicle Screw System	913-5040	FDA UDI	Class II	Active
Indy	1020-34261620	FDA UDI	Class II	Active
Indy	FA42301616T	FDA UDI	Class II	Active
Brickyard	1020-32241212	FDA UDI	Class II	Active
Indy	1030-42302517	FDA UDI	Class II	Active
Indy Standalone	1030-0235	FDA UDI	Class II	Active
Altus Spine HA Pedicle Screw System	811-4530HA	FDA UDI	Class II	Active
Brickyard Stand-Alone ALIF	1030-0302	FDA UDI	Class I	Active
Valencia Pedicle Screw System	980-7570	FDA UDI	Class II	Active
Brickyard ALIF	FA32242517	FDA UDI	Class II	Active
Brickyard	1020-38271210	FDA UDI	Class II	Active
Imola Titanium Interbody Fusion System	F02250-10T	FDA UDI	Class II	Active
Indy Standalone	SL38272013T	FDA UDI	Class II	Active
Silverstone Titanium Interbody Fusion System	SP301011T	FDA UDI	Class II	Active
Altus Spine Interbody Fusion System	1000-0300SB	FDA UDI	Class II	Active
Sochi	A16-18-0020	FDA UDI	Class II	Active
Indy Standalone	SLV4220	FDA UDI	Class II	Active
Altus Spine HA Pedicle Screw System	822-8535HA	FDA UDI	Class II	Active
Imola Titanium Interbody Fusion System	F13040-10T	FDA UDI	Class II	Active
Altus Spine Interbody Fusion System	790-0015	FDA UDI	Class II	Active
Indy	FA42301613T	FDA UDI	Class II	Active
Indy Standalone	1030-2235A	FDA UDI	Class I	Active
Valencia Pedicle Screw System	942-8535	FDA UDI	Class II	Unknown
Monza Cervical Plate System	116-0235	FDA UDI	Class II	Active
Fuji Cervical Plate System	114-0471	FDA UDI	Class II	Active
Silverstone Titanium Interbody Fusion System	ST02206T2	FDA UDI	Class II	Active
Indy	FA32242516	FDA UDI	Class II	Active
Suzuka Interbody Fusion System	ALR005	FDA UDI	Class II	Active
Valencia Pedicle Screw System	942-7545	FDA UDI	Class II	Unknown
Brickyard Stand-Alone ALIF	SL42302519	FDA UDI	Class II	Active
Brickyard	1020-34261210	FDA UDI	Class II	Active
Valencia Pedicle Screw System	943-7525	FDA UDI	Class II	Active

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