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

Catalogue (5998)

Page 29 of 120

Device	Model / Reference	Registries	Class	Status
Brickyard ALIF	FA32240815T	FDA UDI	Class II	Active
Brickyard ALIF	FA32240814	FDA UDI	Class II	Active
Fuji Cervical Plate System	114-0356	FDA UDI	Class II	Active
Brickyard ALIF	FA42301619	FDA UDI	Class II	Active
Altus Spine Interbody Fusion System	1001-1808	FDA UDI	Class II	Active
Monaco Pedicle Screw System	921-6070	FDA UDI	Class II	Active
Monaco Pedicle Screw System	921-6115	FDA UDI	Class II	Active
Monaco Pedicle Screw System	901-5180	FDA UDI	Class II	Active
Fuji Cervical Plate System	136-4020	FDA UDI	Class II	Active
Imola-Silverstone	730-0003	FDA UDI	Class II	Active
Monaco Pedicle Screw System	901-6070	FDA UDI	Class II	Active
Altus Spine Pedicle Screw System	908-1045	FDA UDI	Class II	Active
Suzuka Interbody Fusion System	ALR027	FDA UDI	Class II	Active
Altus Spine Pedicle Screw System	908-1065	FDA UDI	Class II	Active
Monaco Pedicle Screw System	811-4540	FDA UDI	Class II	Active
Indy	FA38271614	FDA UDI	Class II	Active
Altus Spine Interbody Fusion System	730-0010	FDA UDI	Class II	Active
Monaco Pedicle Screw System	931-5110	FDA UDI	Class II	Active
Altus Spine Interbody Fusion System	1000-1814	FDA UDI	Class II	Active
Silverstone Interbody Fusion System	SEC00932-15	FDA UDI	Class II	Active
Fuji Cervical Plate System	111-4320	FDA UDI	Class II	Active
Brickyard ALIF	FA32242012	FDA UDI	Class II	Active
Altus Spine Cervical Interbody Fusion System	210-3109	FDA UDI	Class II	Active
Brickyard Stand-Alone ALIF	1030-4013	FDA UDI	Class I	Active
Valencia Pedicle Screw System	916-3035	FDA UDI	Class II	Active
Monaco Uni-Planar	813-9555	FDA UDI	Class II	Active
Suzuka Interbody Fusion System	ALR004	FDA UDI	Class II	Active
Silverstone Titanium Interbody Fusion System	SP221009T2	FDA UDI	Class II	Active
Fuji Cervical Plate System	121-4315	FDA UDI	Class II	Active
Altus Spine Pedicle Screw System	990-4133TS	FDA UDI	Class II	Active
Indy Standalone	SL42302518	FDA UDI	Class II	Active
Altus Spine Interbody Fusion System	790-0012	FDA UDI	Class II	Active
Indy Standalone	SL42301219T	FDA UDI	Class II	Active
Monaco Pedicle Screw System	902-6090	FDA UDI	Class II	Active
Altus Spine Pedicle Screw System	908-4033T	FDA UDI	Class II	Active
Altus Spine Interbody Fusion System	1000-2612	FDA UDI	Class II	Active
Imola Titanium Interbody Fusion System	F12260-16T	FDA UDI	Class II	Active
Indy	1020-42301615	FDA UDI	Class II	Active
Indy	FA34261614T	FDA UDI	Class II	Active
Indy	1030-0819	FDA UDI	Class I	Active
Monaco Pedicle Screw System	922-5040	FDA UDI	Class II	Active
Monaco Pedicle Screw System	941-5400	FDA UDI	Class II	Active
Valencia Pedicle Screw System	993-6555	FDA UDI	Class II	Active
Indy	1030-1620	FDA UDI	Class I	Active
Indy	1020-1219	FDA UDI	Class II	Active
Monaco Pedicle Screw System	932-5140	FDA UDI	Class II	Active
Imola-Silverstone	790-0038	FDA UDI	Class II	Active
Indy	FA34262517T	FDA UDI	Class II	Active
Altus Spine Interbody Fusion System	722-1018	FDA UDI	Class II	Active
Indy Standalone	SL38270817T	FDA UDI	Class II	Active

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