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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 107 of 120

Device	Model / Reference	Registries	Class	Status
Brickyard	1030-32241616	FDA UDI	Class II	Active
Altus Spine Interbody Fusion System	790-0011	FDA UDI	Class II	Active
Altus Spine Pedicle Screw System	908-1085F	FDA UDI	Class II	Active
Monza Cervical Plate System	116-0368	FDA UDI	Class II	Active
Indy	FA34260814	FDA UDI	Class II	Active
Valencia Pedicle Screw System	973-4530	FDA UDI	Class II	Active
Indy	FA38272515T	FDA UDI	Class II	Active
Altus Spine Interbody Fusion System	1001-2614	FDA UDI	Class II	Active
Indy	1020-34260811	FDA UDI	Class II	Active
Indy Standalone	SL32242017T	FDA UDI	Class II	Active
Altus Spine Pedicle Screw System	908-1045F	FDA UDI	Class II	Active
Altus Spine Interbody Fusion System	1001-2208	FDA UDI	Class II	Active
Monaco Pedicle Screw System	811-1090	FDA UDI	Class II	Active
Imola Titanium Interbody Fusion System	F13040-12T	FDA UDI	Class II	Active
Monaco Pedicle Screw System	931-6045	FDA UDI	Class II	Active
Valencia Pedicle Screw System	975-8545	FDA UDI	Class II	Active
Silverstone Titanium Interbody Fusion System	SP221017T	FDA UDI	Class II	Active
Indy	FA34260820	FDA UDI	Class II	Active
Monaco Pedicle Screw System	922-5150	FDA UDI	Class II	Active
Fuji Cervical Plate System	138-4018	FDA UDI	Class II	Active
Brickyard Stand-Alone ALIF	1030-3220G-45	FDA UDI	Class I	Active
Altus Spine Interbody Fusion System	1001-3010	FDA UDI	Class II	Active
Monaco Pedicle Screw System	922-5175	FDA UDI	Class II	Active
Monza Cervical Plate System	110-4016	FDA UDI	Class II	Active
Brickyard ALIF	FA42302016T	FDA UDI	Class II	Active
Silverstone Titanium Interbody Fusion System	ST52812	FDA UDI	Class II	Active
Valencia Pedicle Screw System	925-4545	FDA UDI	Class II	Unknown
Indy Standalone	SL38271619T	FDA UDI	Class II	Active
Indy	FA32240810	FDA UDI	Class II	Active
Monaco Pedicle Screw System	811-1080	FDA UDI	Class II	Active
Monaco Pedicle Screw System	922-5095	FDA UDI	Class II	Active
Valencia Pedicle Screw System	990-8600	FDA UDI	Class II	Active
Valencia Pedicle Screw System	943-5540	FDA UDI	Class II	Active
Brickyard ALIF	FA38272519T	FDA UDI	Class II	Active
Indy	1030-42301620	FDA UDI	Class II	Active
Valencia Pedicle Screw System	930-8525	FDA UDI	Class II	Active
Valencia Pedicle Screw System	922-7525	FDA UDI	Class II	Unknown
Imola Titanium Interbody Fusion System	F02645-10T	FDA UDI	Class II	Active
Valencia Pedicle Screw System	940-8540	FDA UDI	Class II	Active
Indy	1030-38271217	FDA UDI	Class II	Active
Altus Spine HA Pedicle Screw System	811-7540HA	FDA UDI	Class II	Active
Indy	1030-0012	FDA UDI	Class II	Active
Valencia Pedicle Screw System	909-1075	FDA UDI	Class II	Active
Monaco Pedicle Screw System	931-6115	FDA UDI	Class II	Active
Imola-Silverstone	700-1030	FDA UDI	Class II	Active
Altus Spine Pedicle Screw System	900-1038	FDA UDI	Class II	Active
Monaco Uni-Planar	813-9545	FDA UDI	Class II	Active
Silverstone Titanium Interbody Fusion System	ST83212T	FDA UDI	Class II	Active
Valencia Pedicle Screw System	940-6555	FDA UDI	Class II	Active
Monaco Pedicle Screw System	921-5175	FDA UDI	Class II	Active

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