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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 27 of 120

Device	Model / Reference	Registries	Class	Status
Indy Standalone	1030-0240G-45	FDA UDI	Class II	Active
Silverstone Titanium Interbody Fusion System	ST83214T	FDA UDI	Class II	Active
Brickyard Stand-Alone ALIF	1030-4240	FDA UDI	Class II	Active
Indy Standalone	SL38272515T	FDA UDI	Class II	Active
Brickyard	1020-32240815	FDA UDI	Class II	Active
Altus Spine HA Pedicle Screw System	822-6555HA	FDA UDI	Class II	Active
Monaco Pedicle Screw System	822-7555	FDA UDI	Class II	Active
Indy Standalone	1030-0411	FDA UDI	Class I	Active
Brickyard Stand-Alone ALIF	1030-2220A	FDA UDI	Class I	Active
Silverstone Interbody Fusion System	PS-221007	FDA UDI	Class II	Active
Monaco Pedicle Screw System	922-5110	FDA UDI	Class II	Active
Brickyard ALIF	FA38270810T	FDA UDI	Class II	Active
Indy	1030-32240817	FDA UDI	Class II	Active
Indy	FA42300810T	FDA UDI	Class II	Active
Indy	1030-42301613	FDA UDI	Class II	Active
Valencia Pedicle Screw System	950-8555	FDA UDI	Class II	Active
Valencia Pedicle Screw System	942-7555	FDA UDI	Class II	Unknown
Valencia Pedicle Screw System	925-7545	FDA UDI	Class II	Unknown
Brickyard ALIF	FA34260818T	FDA UDI	Class II	Active
Monaco Pedicle Screw System	932-6115	FDA UDI	Class II	Active
Monaco Pedicle Screw System	932-5145	FDA UDI	Class II	Active
Monaco Pedicle Screw System	921-5105	FDA UDI	Class II	Active
Brickyard ALIF	1020-42301211	FDA UDI	Class II	Active
Monaco Pedicle Screw System	921-6160	FDA UDI	Class II	Active
Imola-Silverstone	1000-0408	FDA UDI	Class II	Active
Monaco Pedicle Screw System	922-6170	FDA UDI	Class II	Active
Altus Spine Interbody Fusion System	1001-2210	FDA UDI	Class II	Active
Suzuka Interbody Fusion System	S730006T	FDA UDI	Class II	Active
Silverstone Titanium Interbody Fusion System	ST82206T2	FDA UDI	Class II	Active
Indy	1030-2615A	FDA UDI	Class I	Active
Brickyard Stand-Alone ALIF	SL42302020T	FDA UDI	Class II	Active
Indy	1020-32240819	FDA UDI	Class II	Active
Monaco Pedicle Screw System	901-5040	FDA UDI	Class II	Active
Valencia Pedicle Screw System	942-7550	FDA UDI	Class II	Unknown
Valencia Pedicle Screw System	973-7550	FDA UDI	Class II	Active
Monaco Pedicle Screw System	932-5045	FDA UDI	Class II	Active
Monaco Pedicle Screw System	911-6040	FDA UDI	Class II	Active
Monaco Pedicle Screw System	922-5050	FDA UDI	Class II	Active
Valencia Pedicle Screw System	940-8585	FDA UDI	Class II	Active
Brickyard ALIF	FA38270817	FDA UDI	Class II	Active
Indy	FA38271213T	FDA UDI	Class II	Active
Valencia Pedicle Screw System	900-1012	FDA UDI	Class II	Active
Monza Cervical Plate System	116-0238	FDA UDI	Class II	Active
Fuji Cervical Plate System	111-4012	FDA UDI	Class II	Active
Valencia Pedicle Screw System	983-5550	FDA UDI	Class II	Active
Altus Spine Interbody Fusion System	722-1012	FDA UDI	Class II	Active
Valencia Pedicle Screw System	980-7595	FDA UDI	Class II	Active
Suzuka Interbody Fusion System	ALR108	FDA UDI	Class II	Active
Indy	FA32241612	FDA UDI	Class II	Active
Brickyard ALIF	FA42301617	FDA UDI	Class II	Active

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