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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 110 of 120

Device	Model / Reference	Registries	Class	Status
Altus Spine Pedicle Screw System	908-4115	FDA UDI	Class II	Active
Altus Spine Pedicle Screw System	900-1034	FDA UDI	Class II	Active
Valencia Pedicle Screw System	973-7585	FDA UDI	Class II	Active
Brickyard Stand-Alone ALIF	1030-0240	FDA UDI	Class II	Active
Imola Interbody Fusion System	F11855-10	FDA UDI	Class II	Active
Monaco Uni-Planar	880-5316	FDA UDI	Class II	Active
Indy	FA38271220	FDA UDI	Class II	Active
Silverstone Titanium Interbody Fusion System	SP261014T2	FDA UDI	Class II	Active
Valencia Pedicle Screw System	975-8565	FDA UDI	Class II	Active
Altus Spine Cervical Interbody Fusion System	210-3110	FDA UDI	Class II	Active
Monaco Pedicle Screw System	921-6080	FDA UDI	Class II	Active
Brickyard Stand-Alone ALIF	SL32241211	FDA UDI	Class II	Active
Sochi	A16-33-0205	FDA UDI	Class II	Active
Brickyard Stand-Alone ALIF	SL0020	FDA UDI	Class II	Active
Imola Interbody Fusion System	F02645-14	FDA UDI	Class II	Active
Suzuka Interbody Fusion System	ALR824	FDA UDI	Class II	Active
Sochi	A16-13-4022	FDA UDI	Class II	Active
Imola Interbody Fusion System	F02650-14	FDA UDI	Class II	Active
Valencia Pedicle Screw System	970-4545	FDA UDI	Class II	Active
Valencia Pedicle Screw System	950-8525	FDA UDI	Class II	Active
Valencia Pedicle Screw System	925-5555	FDA UDI	Class II	Unknown
Monaco Pedicle Screw System	901-5080	FDA UDI	Class II	Active
Imola-Silverstone	1000-0414	FDA UDI	Class II	Active
Valencia Pedicle Screw System	940-6575	FDA UDI	Class II	Active
Silverstone Titanium Interbody Fusion System	ST52808T	FDA UDI	Class II	Active
Imola Titanium Interbody Fusion System	F11850-16T	FDA UDI	Class II	Active
Valencia Pedicle Screw System	973-8595	FDA UDI	Class II	Active
Brickyard ALIF	FA32242019T	FDA UDI	Class II	Active
Indy	FA42302015	FDA UDI	Class II	Active
Indy	1030-42301619	FDA UDI	Class II	Active
Valencia Pedicle Screw System	9000-1004	FDA UDI	Class II	Active
Sochi	A16-12-4030	FDA UDI	Class II	Active
Indy Standalone	SL38270814	FDA UDI	Class II	Active
Valencia Pedicle Screw System	925-8540	FDA UDI	Class II	Unknown
Brickyard ALIF	FA38271220T	FDA UDI	Class II	Active
Indy	1020-1212	FDA UDI	Class II	Active
Valencia Pedicle Screw System	950-6555	FDA UDI	Class II	Active
Valencia Pedicle Screw System	993-5555	FDA UDI	Class II	Active
Imola Interbody Fusion System	F02640-12	FDA UDI	Class II	Active
Brickyard ALIF	FA32242018	FDA UDI	Class II	Active
Brickyard ALIF	FA42301214	FDA UDI	Class II	Active
Valencia Pedicle Screw System	925-8560	FDA UDI	Class II	Unknown
Valencia Pedicle Screw System	925-4550	FDA UDI	Class II	Unknown
Valencia Pedicle Screw System	924-5640	FDA UDI	Class II	Active
Sochi	A16-21-1806	FDA UDI	Class II	Active
Brickyard Stand-Alone ALIF	SL32241211T	FDA UDI	Class II	Active
Suzuka Interbody Fusion System	S420008T	FDA UDI	Class II	Active
Monaco Pedicle Screw System	912-6180	FDA UDI	Class II	Active
Monaco Pedicle Screw System	822-7620	FDA UDI	Class II	Active
Monaco Pedicle Screw System	922-6175	FDA UDI	Class II	Active

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