Is this your brand? Sign in to claim ownership.

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 91 of 120

Device	Model / Reference	Registries	Class	Status
Suzuka Interbody Fusion System	ALR17-004	FDA UDI	Class II	Active
Monaco Pedicle Screw System	932-5165	FDA UDI	Class II	Active
Imola Interbody Fusion System	F62650-08	FDA UDI	Class II	Active
Valencia Pedicle Screw System	970-8600	FDA UDI	Class II	Active
Indy	1020-38270810	FDA UDI	Class II	Active
Altus Spine Pedicle Screw System	880-1095C	FDA UDI	Class II	Active
Fuji Cervical Plate System	100-1030	FDA UDI	Class II	Active
Altus Spine Interbody Fusion System	722-1009	FDA UDI	Class II	Active
Brickyard	1020-42301619	FDA UDI	Class II	Active
Altus Spine Interbody Fusion System	722-1014	FDA UDI	Class II	Active
Indy Standalone	SL42300813T	FDA UDI	Class II	Active
Valencia Pedicle Screw System	900-1041	FDA UDI	Class II	Active
Indy	1020-38271218	FDA UDI	Class II	Active
Valencia Pedicle Screw System	970-4530	FDA UDI	Class II	Active
Monaco Pedicle Screw System	931-6060	FDA UDI	Class II	Active
Brickyard	1020-32242519	FDA UDI	Class II	Active
Fuji Cervical Plate System	122-4314	FDA UDI	Class II	Active
Valencia Pedicle Screw System	975-8540	FDA UDI	Class II	Active
Brickyard Stand-Alone ALIF	SL32241219	FDA UDI	Class II	Active
Indy Standalone	SL38272020	FDA UDI	Class II	Active
Brickyard Stand-Alone ALIF	1030-4220	FDA UDI	Class II	Active
Valencia Pedicle Screw System	923-5050	FDA UDI	Class II	Active
Indy Standalone	SL38270815	FDA UDI	Class II	Active
Imola Titanium Interbody Fusion System	F11850-14T	FDA UDI	Class II	Active
Altus Spine HA Pedicle Screw System	822-8590HA	FDA UDI	Class II	Active
Altus Spine HA Pedicle Screw System	822-9530HA	FDA UDI	Class II	Active
Indy Standalone	SL38270815T	FDA UDI	Class II	Active
Indy	FA32240812	FDA UDI	Class II	Active
Valencia Pedicle Screw System	909-0001	FDA UDI	Class II	Active
Imola Titanium Interbody Fusion System	F12240-16T	FDA UDI	Class II	Active
Silverstone Interbody Fusion System	PS-261012	FDA UDI	Class II	Active
Brickyard	1030-32242520	FDA UDI	Class II	Active
Valencia Pedicle Screw System	900-1042	FDA UDI	Class II	Active
Altus Spine Pedicle Screw System	975-0007	FDA UDI	Class II	Active
Suzuka Interbody Fusion System	ALR107	FDA UDI	Class II	Active
Monza Cervical Plate System	120-4018	FDA UDI	Class II	Active
Imola Interbody Fusion System	F01850-08	FDA UDI	Class II	Active
Imola Interbody Fusion System	F12660-14	FDA UDI	Class II	Active
Brickyard	1020-38272020	FDA UDI	Class II	Active
Brickyard Stand-Alone ALIF	SL42300815	FDA UDI	Class II	Active
Monaco Pedicle Screw System	901-5400	FDA UDI	Class II	Active
Brickyard ALIF	FA34260812	FDA UDI	Class II	Active
Altus Spine Pedicle Screw System	908-0075TS	FDA UDI	Class II	Active
Imola-Silverstone	1000-0734	FDA UDI	Class II	Active
Altus Spine Interbody Fusion System	1000-1816	FDA UDI	Class II	Active
Indy Standalone	SL32241214	FDA UDI	Class II	Active
Brickyard Stand-Alone ALIF	1030-3016	FDA UDI	Class I	Active
Brickyard Stand-Alone ALIF	SL32241216T	FDA UDI	Class II	Active
Brickyard ALIF	FA38270812T	FDA UDI	Class II	Active
Silverstone Titanium Interbody Fusion System	ST02813T	FDA UDI	Class II	Active

Related Companies

Authorised Representatives

No authorised representatives on record.

Importers

Not available yet.

Notified Bodies

Not available yet.

Authorities

Not available yet.