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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 85 of 120

Device	Model / Reference	Registries	Class	Status
Valencia Pedicle Screw System	993-8600	FDA UDI	Class II	Active
Brickyard ALIF	FA34261220T	FDA UDI	Class II	Active
Brickyard ALIF	FA32241210	FDA UDI	Class II	Active
Valencia Pedicle Screw System	913-5160	FDA UDI	Class II	Active
Silverstone Titanium Interbody Fusion System	ST82210T	FDA UDI	Class II	Active
Silverstone Titanium Interbody Fusion System	ST02214T2	FDA UDI	Class II	Active
Valencia Pedicle Screw System	970-8590	FDA UDI	Class II	Active
Fuji Cervical Plate System	138-4013	FDA UDI	Class II	Active
Altus Spine Pedicle Screw System	908-1055	FDA UDI	Class II	Active
Monza Cervical Plate System	110-4318	FDA UDI	Class II	Active
Valencia Pedicle Screw System	943-8590	FDA UDI	Class II	Active
Valencia Pedicle Screw System	970-7530	FDA UDI	Class II	Active
Sochi	A16-12-4010	FDA UDI	Class II	Active
Brickyard	1030-0808	FDA UDI	Class I	Active
Brickyard	1020-38272516	FDA UDI	Class II	Active
Monza Cervical Plate System	116-0362	FDA UDI	Class II	Active
Brickyard	1030-38271219	FDA UDI	Class II	Active
Monaco Pedicle Screw System	932-6140	FDA UDI	Class II	Active
Monaco Pedicle Screw System	912-5180	FDA UDI	Class II	Active
Silverstone Titanium Interbody Fusion System	ST53208T2	FDA UDI	Class II	Active
Suzuka Interbody Fusion System	S410509T	FDA UDI	Class II	Active
Valencia Pedicle Screw System	944-0030	FDA UDI	Class II	Unknown
Valencia Pedicle Screw System	980-6550	FDA UDI	Class II	Active
Monaco Pedicle Screw System	822-7590	FDA UDI	Class II	Active
Indy	1030-32240810	FDA UDI	Class II	Active
Brickyard ALIF	FA38271220	FDA UDI	Class II	Active
Monaco Pedicle Screw System	931-6135	FDA UDI	Class II	Active
Indy	1030-2020	FDA UDI	Class I	Active
Brickyard ALIF	FA42301219	FDA UDI	Class II	Active
Sochi	A16-12-4515	FDA UDI	Class II	Active
Suzuka Interbody Fusion System	S421004	FDA UDI	Class II	Active
Sochi	A16-12-3514	FDA UDI	Class II	Active
Imola-Silverstone	700-0030	FDA UDI	Class II	Active
Indy	FA38271217	FDA UDI	Class II	Active
Monaco Pedicle Screw System	902-5180	FDA UDI	Class II	Active
Indy	1020-42301217	FDA UDI	Class II	Active
Monaco Pedicle Screw System	921-5035	FDA UDI	Class II	Active
Monaco Pedicle Screw System	911-5400	FDA UDI	Class II	Active
PEEK Interbody Fusion System	TL22009	FDA UDI	Class II	Active
Valencia Pedicle Screw System	942-6535	FDA UDI	Class II	Unknown
Valencia Pedicle Screw System	913-5435	FDA UDI	Class II	Active
Valencia Pedicle Screw System	990-4560	FDA UDI	Class II	Active
PSS-Pedicle Screw System	900-1065	FDA UDI	Class II	Unknown
Indy	FA34260812T	FDA UDI	Class II	Active
Indy Standalone	SL42302019T	FDA UDI	Class II	Active
Altus Spine Interbody Fusion System	730-0012	FDA UDI	Class II	Active
Monza Cervical Plate System	116-0350	FDA UDI	Class II	Active
Monaco Pedicle Screw System	822-8550	FDA UDI	Class II	Active
Silverstone Titanium Interbody Fusion System	SP221018T	FDA UDI	Class II	Active
Valencia Pedicle Screw System	922-6530	FDA UDI	Class II	Unknown

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