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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: —
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Phone: —
PRRC Contact: —
EUDAMED SRN: —
FDA FEI Number: —
DUNS Number: —

Catalogue (5998)

Page 97 of 120

Device	Model / Reference	Registries	Class	Status
Monza Cervical Plate System	135-4320	FDA UDI	Class II	Active
Indy	1030-38270814	FDA UDI	Class II	Active
Monaco Pedicle Screw System	932-5180	FDA UDI	Class II	Active
Indy	1020-32241212	FDA UDI	Class II	Active
Indy Standalone	SL32241619T	FDA UDI	Class II	Active
Altus Spine Interbody Fusion System	1000-2206	FDA UDI	Class II	Active
Brickyard ALIF	FA32240810T	FDA UDI	Class II	Active
Suzuka Interbody Fusion System	S410506T	FDA UDI	Class II	Active
Monaco Pedicle Screw System	901-5110	FDA UDI	Class II	Active
Indy	FA38270819T	FDA UDI	Class II	Active
Monza Cervical Plate System	116-0241	FDA UDI	Class II	Active
Monaco Pedicle Screw System	811-6540	FDA UDI	Class II	Active
Sochi	A16-24-0020	FDA UDI	Class II	Active
Silverstone Interbody Fusion System	PS-261015	FDA UDI	Class II	Active
Valencia Pedicle Screw System	915-1911	FDA UDI	Class II	Active
Silverstone Titanium Interbody Fusion System	ST52807T2	FDA UDI	Class II	Active
Imola Interbody Fusion System	F02655-08	FDA UDI	Class II	Active
Suzuka Interbody Fusion System	ALR525	FDA UDI	Class II	Active
Indy	FA38270815T	FDA UDI	Class II	Active
Monaco Pedicle Screw System	922-6065	FDA UDI	Class II	Active
Valencia Pedicle Screw System	923-5115	FDA UDI	Class II	Active
Imola Interbody Fusion System	F02240-16	FDA UDI	Class II	Active
Valencia Pedicle Screw System	983-5525	FDA UDI	Class II	Active
Imola Titanium Interbody Fusion System	F01860-08T	FDA UDI	Class II	Active
Valencia Pedicle Screw System	970-5535	FDA UDI	Class II	Active
Valencia Pedicle Screw System	930-6550	FDA UDI	Class II	Active
Altus Spine HA Pedicle Screw System	811-8525HA	FDA UDI	Class II	Active
Monaco Pedicle Screw System	931-6065	FDA UDI	Class II	Active
Indy	1030-38271615	FDA UDI	Class II	Active
Valencia Pedicle Screw System	973-7575	FDA UDI	Class II	Active
Valencia Pedicle Screw System	940-7590	FDA UDI	Class II	Active
Brickyard Stand-Alone ALIF	1030-2140A	FDA UDI	Class I	Active
Indy Standalone	SL32241218	FDA UDI	Class II	Active
Sochi	A16-32-4511	FDA UDI	Class II	Active
Valencia Pedicle Screw System	930-5530	FDA UDI	Class II	Active
Suzuka Interbody Fusion System	S730011T	FDA UDI	Class II	Active
Indy	1030-32242517	FDA UDI	Class II	Active
Valencia Pedicle Screw System	943-6570	FDA UDI	Class II	Active
Brickyard	1020-32241209	FDA UDI	Class II	Active
Fuji Cervical Plate System	114-0253	FDA UDI	Class II	Active
Indy Standalone	SL38272017T	FDA UDI	Class II	Active
Valencia Pedicle Screw System	913-5035	FDA UDI	Class II	Active
Indy Standalone	SL38271614	FDA UDI	Class II	Active
Indy	FA32241219T	FDA UDI	Class II	Active
Indy	FA32241217	FDA UDI	Class II	Active
Monaco Pedicle Screw System	942-6400	FDA UDI	Class II	Active
Brickyard Stand-Alone ALIF	SL32242517	FDA UDI	Class II	Active
Suzuka Interbody Fusion System	S730507T	FDA UDI	Class II	Active
Silverstone Interbody Fusion System	PS-301015	FDA UDI	Class II	Active
Valencia Pedicle Screw System	980-7565	FDA UDI	Class II	Active

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