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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 98 of 120

Device	Model / Reference	Registries	Class	Status
Valencia Pedicle Screw System	993-8585	FDA UDI	Class II	Active
Silverstone Interbody Fusion System	PS-221011	FDA UDI	Class II	Active
Indy Standalone	1030-3010	FDA UDI	Class I	Active
Valencia Pedicle Screw System	975-6570	FDA UDI	Class II	Active
Fuji Cervical Plate System	114-0126	FDA UDI	Class II	Active
Brickyard	1020-34261612	FDA UDI	Class II	Active
Imola Titanium Interbody Fusion System	F13060-12T	FDA UDI	Class II	Active
Imola Titanium Interbody Fusion System	F12655-10T	FDA UDI	Class II	Active
Valencia Pedicle Screw System	950-7535	FDA UDI	Class II	Active
Imola Titanium Interbody Fusion System	F01845-14T	FDA UDI	Class II	Active
Monaco Pedicle Screw System	921-5180	FDA UDI	Class II	Active
Fuji Cervical Plate System	112-4014	FDA UDI	Class II	Active
Brickyard Stand-Alone ALIF	SLV4215	FDA UDI	Class II	Active
Indy Standalone	SL38271614T	FDA UDI	Class II	Active
Indy	FA42300819	FDA UDI	Class II	Active
Valencia Pedicle Screw System	908-1202	FDA UDI	Class II	Active
Sochi	A16-22-4535	FDA UDI	Class II	Active
Imola Titanium Interbody Fusion System	F02250-12T	FDA UDI	Class II	Active
Valencia Pedicle Screw System	983-5545	FDA UDI	Class II	Active
Brickyard	1020-34261213	FDA UDI	Class II	Active
Valencia Pedicle Screw System	973-6560	FDA UDI	Class II	Active
Brickyard ALIF	FA34260813T	FDA UDI	Class II	Active
Indy	FA38270815	FDA UDI	Class II	Active
Sochi	A16-12-4022	FDA UDI	Class II	Active
Valencia Pedicle Screw System	940-7585	FDA UDI	Class II	Active
Sochi	A16-10-4024	FDA UDI	Class II	Active
Valencia Pedicle Screw System	980-5565	FDA UDI	Class II	Active
Brickyard	1030-1216	FDA UDI	Class I	Active
Indy	FA32241219	FDA UDI	Class II	Active
Imola Titanium Interbody Fusion System	F01845-10T	FDA UDI	Class II	Active
Brickyard ALIF	FA32242518	FDA UDI	Class II	Active
Valencia Pedicle Screw System	940-6525	FDA UDI	Class II	Active
Altus Spine Interbody Fusion System	1000-1810	FDA UDI	Class II	Active
Monaco Pedicle Screw System	901-5120	FDA UDI	Class II	Active
Brickyard Stand-Alone ALIF	1030-4015	FDA UDI	Class I	Active
Indy	FA34261613T	FDA UDI	Class II	Active
Altus Spine Pedicle Screw System	908-1065F	FDA UDI	Class II	Active
Monaco Pedicle Screw System	922-5090	FDA UDI	Class II	Active
Monaco Pedicle Screw System	901-6140	FDA UDI	Class II	Active
Indy Standalone	1030-0220	FDA UDI	Class II	Active
Brickyard ALIF	FA34260811	FDA UDI	Class II	Active
Altus Spine Cervical Interbody Fusion System	210-1006	FDA UDI	Class II	Active
Valencia Pedicle Screw System	975-8580	FDA UDI	Class II	Active
Altus Spine Cervical Interbody Fusion System	210-1007	FDA UDI	Class II	Active
Altus Spine Interbody Fusion System	1000-1806B	FDA UDI	Class II	Active
Valencia Pedicle Screw System	990-5555	FDA UDI	Class II	Active
Valencia Pedicle Screw System	913- 5140M	FDA UDI	Class II	Active
Imola Titanium Interbody Fusion System	F03055-12T	FDA UDI	Class II	Active
Sochi	A16-32-4510	FDA UDI	Class II	Active
Monaco Pedicle Screw System	811-8590	FDA UDI	Class II	Active

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