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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 22 of 120

Device	Model / Reference	Registries	Class	Status
Imola Titanium Interbody Fusion System	F01860-14T	FDA UDI	Class II	Active
Valencia Pedicle Screw System	922-4535	FDA UDI	Class II	Unknown
Monaco Pedicle Screw System	902-6040	FDA UDI	Class II	Active
Valencia Pedicle Screw System	960-5550	FDA UDI	Class II	Unknown
Brickyard	1030-1218	FDA UDI	Class I	Active
Indy	1030-0017	FDA UDI	Class II	Active
Monaco Pedicle Screw System	811-4555	FDA UDI	Class II	Active
Altus Spine Pedicle Screw System	900-1122	FDA UDI	Class II	Active
Monaco Pedicle Screw System	932-5085	FDA UDI	Class II	Active
Valencia Pedicle Screw System	909-1085	FDA UDI	Class II	Active
Sochi	A16-32-4513	FDA UDI	Class II	Active
Silverstone Titanium Interbody Fusion System	ST03207T2	FDA UDI	Class II	Active
Valencia Pedicle Screw System	993-7580	FDA UDI	Class II	Active
Silverstone Titanium Interbody Fusion System	ST52208T	FDA UDI	Class II	Active
Valencia Pedicle Screw System	990-8575	FDA UDI	Class II	Active
Valencia Pedicle Screw System	942-6530	FDA UDI	Class II	Unknown
Valencia Pedicle Screw System	950-7530	FDA UDI	Class II	Active
Valencia Pedicle Screw System	940-6560	FDA UDI	Class II	Active
Altus Spine Pedicle Screw System	908-1058TS	FDA UDI	Class II	Active
Valencia Pedicle Screw System	980-7580	FDA UDI	Class II	Active
Altus Spine Interbody Fusion System	722-1007	FDA UDI	Class II	Active
Valencia Pedicle Screw System	975-8550	FDA UDI	Class II	Active
Valencia Pedicle Screw System	925-4540	FDA UDI	Class II	Unknown
Monaco Uni-Planar	831-1003	FDA UDI	Class II	Active
Imola-Silverstone	600-3103	FDA UDI	Class II	Active
Suzuka Interbody Fusion System	S730510	FDA UDI	Class II	Active
Monaco Pedicle Screw System	901-5090	FDA UDI	Class II	Active
Valencia Pedicle Screw System	940-7565	FDA UDI	Class II	Active
Monaco Pedicle Screw System	811-8580	FDA UDI	Class II	Active
Monaco Uni-Planar	831-1601	FDA UDI	Class II	Active
Sochi	A10-24-1425	FDA UDI	Class II	Active
Valencia Pedicle Screw System	973-6565	FDA UDI	Class II	Active
Imola Titanium Interbody Fusion System	F01840-10T	FDA UDI	Class II	Active
Brickyard Stand-Alone ALIF	1030-3017	FDA UDI	Class I	Active
Suzuka Interbody Fusion System	S730007	FDA UDI	Class II	Active
Valencia Pedicle Screw System	913-5150	FDA UDI	Class II	Active
Brickyard ALIF	FA38272019	FDA UDI	Class II	Active
Sochi	A16-12-3545	FDA UDI	Class II	Active
Brickyard ALIF	FA32242518T	FDA UDI	Class II	Active
Brickyard Stand-Alone ALIF	SL0017	FDA UDI	Class II	Active
Altus Spine HA Pedicle Screw System	822-5560HA	FDA UDI	Class II	Active
Indy	FA42301218	FDA UDI	Class II	Active
Monza Cervical Plate System	110-4312	FDA UDI	Class II	Active
Monaco Pedicle Screw System	911-6050	FDA UDI	Class II	Active
Indy	1020-32240820	FDA UDI	Class II	Active
Sochi	A10-23-0130	FDA UDI	Class II	Active
Sochi	A16-12-3535	FDA UDI	Class II	Active
Altus Spine HA Pedicle Screw System	822-7570HA	FDA UDI	Class II	Active
Suzuka Interbody Fusion System	S420806T	FDA UDI	Class II	Active
Valencia Pedicle Screw System	990-4550	FDA UDI	Class II	Active

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