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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 87 of 120

Device	Model / Reference	Registries	Class	Status
Altus Spine Pedicle Screw System	990-4133	FDA UDI	Class II	Active
Indy	1030-32242013	FDA UDI	Class II	Active
Brickyard Stand-Alone ALIF	SL0019	FDA UDI	Class II	Active
Altus Spine HA Pedicle Screw System	811-7580HA	FDA UDI	Class II	Active
Indy	1020-34262017	FDA UDI	Class II	Active
Fuji Cervical Plate System	100-2027	FDA UDI	Class II	Active
Valencia Pedicle Screw System	990-4530	FDA UDI	Class II	Active
Valencia Pedicle Screw System	990-4555	FDA UDI	Class II	Active
Valencia Pedicle Screw System	980-6545	FDA UDI	Class II	Active
Silverstone Titanium Interbody Fusion System	ST82807T2	FDA UDI	Class II	Active
Altus Spine HA Pedicle Screw System	811-5040HA	FDA UDI	Class II	Active
Indy	FA32241215T	FDA UDI	Class II	Active
Sochi	A16-18-1035	FDA UDI	Class II	Active
Silverstone Titanium Interbody Fusion System	ST52810	FDA UDI	Class II	Active
Monaco Pedicle Screw System	932-6085	FDA UDI	Class II	Active
Imola Interbody Fusion System	F03040-16	FDA UDI	Class II	Active
Valencia Pedicle Screw System	942-7540	FDA UDI	Class II	Unknown
Indy	FA34262016	FDA UDI	Class II	Active
Brickyard ALIF	FA38271210T	FDA UDI	Class II	Active
Brickyard Stand-Alone ALIF	SL38271620T	FDA UDI	Class II	Active
Brickyard Stand-Alone ALIF	SL42301615T	FDA UDI	Class II	Active
Brickyard Stand-Alone ALIF	SLV4240	FDA UDI	Class II	Active
Brickyard ALIF	FA42301615T	FDA UDI	Class II	Active
Indy	1020-38271614	FDA UDI	Class II	Active
Valencia Pedicle Screw System	942-5530	FDA UDI	Class II	Unknown
Valencia Pedicle Screw System	922-6550	FDA UDI	Class II	Unknown
Indy	1020-38271616	FDA UDI	Class II	Active
Monaco Pedicle Screw System	921-5095	FDA UDI	Class II	Active
Brickyard	1020-32240813	FDA UDI	Class II	Active
Indy Standalone	1030-2240A	FDA UDI	Class I	Active
Altus Spine HA Pedicle Screw System	822-6545HA	FDA UDI	Class II	Active
Valencia Pedicle Screw System	943-6535	FDA UDI	Class II	Active
Brickyard ALIF	1020-42300815	FDA UDI	Class II	Active
Indy	1020-42302016	FDA UDI	Class II	Active
Indy	1020-32240818	FDA UDI	Class II	Active
Silverstone Titanium Interbody Fusion System	ST02816T	FDA UDI	Class II	Active
Brickyard Stand-Alone ALIF	1030-0017	FDA UDI	Class II	Active
Valencia Pedicle Screw System	940-5565	FDA UDI	Class II	Active
Brickyard ALIF	FA34261612	FDA UDI	Class II	Active
Imola-Silverstone	780-0019	FDA UDI	Class II	Active
Valencia Pedicle Screw System	940-5550	FDA UDI	Class II	Active
Brickyard	1030-38271212	FDA UDI	Class II	Active
Indy Standalone	SL38270811	FDA UDI	Class II	Active
Altus Spine HA Pedicle Screw System	822-8555HA	FDA UDI	Class II	Active
Suzuka Interbody Fusion System	S420805	FDA UDI	Class II	Active
Altus Spine Interbody Fusion System	1000-2608	FDA UDI	Class II	Active
Valencia Pedicle Screw System	944-0025	FDA UDI	Class II	Unknown
Silverstone Titanium Interbody Fusion System	ST53209T2	FDA UDI	Class II	Active
Imola Interbody Fusion System	F01850-12	FDA UDI	Class II	Active
Indy Standalone	SL38272516T	FDA UDI	Class II	Active

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