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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 36 of 120

Device	Model / Reference	Registries	Class	Status
Indy Standalone	SL38271218T	FDA UDI	Class II	Active
Valencia Pedicle Screw System	924-5680	FDA UDI	Class II	Active
Indy	FA42301211	FDA UDI	Class II	Active
Imola Titanium Interbody Fusion System	F02250-08T	FDA UDI	Class II	Active
Indy	1030-38271211	FDA UDI	Class II	Active
Indy	1020-32240815	FDA UDI	Class II	Active
Imola-Silverstone	705-3013	FDA UDI	Class II	Active
Indy	FA34261220	FDA UDI	Class II	Active
Monaco Pedicle Screw System	932-5110	FDA UDI	Class II	Active
Indy Standalone	1030-1092	FDA UDI	Class I	Active
Indy	FA42302519T	FDA UDI	Class II	Active
Valencia Pedicle Screw System	943-7570	FDA UDI	Class II	Active
Valencia Pedicle Screw System	942-7560	FDA UDI	Class II	Unknown
Monaco Pedicle Screw System	911-5080	FDA UDI	Class II	Active
Brickyard ALIF	FA34262019T	FDA UDI	Class II	Active
Monaco Pedicle Screw System	901-6080	FDA UDI	Class II	Active
Suzuka Interbody Fusion System	S410805	FDA UDI	Class II	Active
Valencia Pedicle Screw System	943-7530	FDA UDI	Class II	Active
Valencia Pedicle Screw System	943-8600	FDA UDI	Class II	Active
Suzuka Interbody Fusion System	S420504T	FDA UDI	Class II	Active
Imola-Silverstone	600-3130	FDA UDI	Class II	Active
Fuji Cervical Plate System	138-4014	FDA UDI	Class II	Active
Altus Spine Pedicle Screw System	880-1075	FDA UDI	Class II	Active
Monaco Pedicle Screw System	921-5080	FDA UDI	Class II	Active
Altus Spine Interbody Fusion System	722-2006	FDA UDI	Class II	Active
Indy	1020-42302020	FDA UDI	Class II	Active
Monaco Pedicle Screw System	932-6030	FDA UDI	Class II	Active
Brickyard	1030-1118	FDA UDI	Class I	Active
Monaco Pedicle Screw System	901-6160	FDA UDI	Class II	Active
Imola Interbody Fusion System	F02650-10	FDA UDI	Class II	Active
Valencia Pedicle Screw System	924-5595	FDA UDI	Class II	Active
Valencia Pedicle Screw System	925-8535	FDA UDI	Class II	Unknown
Suzuka Interbody Fusion System	ALR808	FDA UDI	Class II	Active
Indy Standalone	SL38272019	FDA UDI	Class II	Active
Brickyard Stand-Alone ALIF	1030-4006	FDA UDI	Class I	Active
Valencia Pedicle Screw System	913- 5220M	FDA UDI	Class II	Active
Imola Interbody Fusion System	F12645-16	FDA UDI	Class II	Active
Valencia Pedicle Screw System	922-8535	FDA UDI	Class II	Unknown
Fuji Cervical Plate System	122-4014	FDA UDI	Class II	Active
Fuji Cervical Plate System	121-4314	FDA UDI	Class II	Active
Brickyard Stand-Alone ALIF	SL38271218	FDA UDI	Class II	Active
Valencia Pedicle Screw System	993-5545	FDA UDI	Class II	Active
Brickyard Stand-Alone ALIF	SL38272018	FDA UDI	Class II	Active
Brickyard	1020-38271618	FDA UDI	Class II	Active
Valencia Pedicle Screw System	942-6540	FDA UDI	Class II	Unknown
Valencia Pedicle Screw System	950-7540	FDA UDI	Class II	Active
Brickyard Stand-Alone ALIF	SL42301212	FDA UDI	Class II	Active
Imola Interbody Fusion System	F12255-16	FDA UDI	Class II	Active
Brickyard	1020-34260818	FDA UDI	Class II	Active
Brickyard Stand-Alone ALIF	SL42301217	FDA UDI	Class II	Active

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