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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 109 of 120

Device	Model / Reference	Registries	Class	Status
Imola Titanium Interbody Fusion System	F11855-12T	FDA UDI	Class II	Active
Indy	FA34261617T	FDA UDI	Class II	Active
Altus Spine Interbody Fusion System	722-1011	FDA UDI	Class II	Active
Monaco Pedicle Screw System	922-5100	FDA UDI	Class II	Active
Monaco Pedicle Screw System	921-5125	FDA UDI	Class II	Active
Indy	FA38272017T	FDA UDI	Class II	Active
Monaco Pedicle Screw System	931-6030	FDA UDI	Class II	Active
Valencia Pedicle Screw System	922-5560	FDA UDI	Class II	Unknown
Suzuka Interbody Fusion System	ALR011	FDA UDI	Class II	Active
Valencia Pedicle Screw System	923-5125	FDA UDI	Class II	Active
Brickyard Stand-Alone ALIF	SL38270815T	FDA UDI	Class II	Active
Indy Standalone	SL32242517	FDA UDI	Class II	Active
Brickyard	1020-42301217	FDA UDI	Class II	Active
Suzuka Interbody Fusion System	ALR830	FDA UDI	Class II	Active
Monza Cervical Plate System	116-0371	FDA UDI	Class II	Active
Brickyard Stand-Alone ALIF	1030-4012	FDA UDI	Class I	Active
Valencia Pedicle Screw System	922-5525	FDA UDI	Class II	Unknown
Monaco Pedicle Screw System	921-6030	FDA UDI	Class II	Active
Suzuka Interbody Fusion System	S730807	FDA UDI	Class II	Active
Monaco Uni-Planar	880-5316C	FDA UDI	Class II	Active
Brickyard ALIF	FA32241618	FDA UDI	Class II	Active
Altus Spine Interbody Fusion System	1000-0300S	FDA UDI	Class II	Active
Altus Spine Pedicle Screw System	908-1055F	FDA UDI	Class II	Active
Imola Interbody Fusion System	FA082430-12	FDA UDI	Class II	Active
Suzuka Interbody Fusion System	S730507	FDA UDI	Class II	Active
Brickyard ALIF	FA32241616T	FDA UDI	Class II	Active
Indy	FA42301613	FDA UDI	Class II	Active
Valencia Pedicle Screw System	990-6525	FDA UDI	Class II	Active
Valencia Pedicle Screw System	970-7545	FDA UDI	Class II	Active
Silverstone Titanium Interbody Fusion System	SP301012T2	FDA UDI	Class II	Active
Indy Standalone	1030-0235G-45	FDA UDI	Class II	Active
Indy	FA32242520	FDA UDI	Class II	Active
Monaco Pedicle Screw System	921-6175	FDA UDI	Class II	Active
Valencia Pedicle Screw System	973-6540	FDA UDI	Class II	Active
Brickyard Stand-Alone ALIF	SL42301617T	FDA UDI	Class II	Active
Indy	1020-38272015	FDA UDI	Class II	Active
Indy	1020-32241615	FDA UDI	Class II	Active
Valencia Pedicle Screw System	940-7560	FDA UDI	Class II	Active
Imola Interbody Fusion System	FA082430-14	FDA UDI	Class II	Active
Valencia Pedicle Screw System	980-8600	FDA UDI	Class II	Active
Indy	1020-42301213	FDA UDI	Class II	Active
Altus Spine Pedicle Screw System	880-1042	FDA UDI	Class II	Active
Altus Spine Cervical Interbody Fusion System	210-0005	FDA UDI	Class II	Active
Monaco Pedicle Screw System	902-6435	FDA UDI	Class II	Active
Imola Interbody Fusion System	F11860-16	FDA UDI	Class II	Active
Monaco Pedicle Screw System	811-8545	FDA UDI	Class II	Active
Altus Spine Pedicle Screw System	908-1075	FDA UDI	Class II	Active
Altus Spine Interbody Fusion System	722-1010	FDA UDI	Class II	Active
Valencia Pedicle Screw System	940-8550	FDA UDI	Class II	Active
Indy	1020-34262516	FDA UDI	Class II	Active

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