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NEUROSTRUCTURES, INC

US

Last updated May 24, 2026

What NEUROSTRUCTURES, INC makes

NeuroStructures, Inc. manufactures orthopaedic and spinal fixation devices, including non-bioabsorbable spinal plates, polymeric interbody fusion cages, and internal fixation systems with screws and plates. Their portfolio also includes reusable positioning instruments for orthopaedic prosthesis implantation and non-sterile bone-screw fixation systems for spinal stabilization.

The company’s devices are classified as Class II under FDA regulations and are listed in the FDA’s Unique Device Identifier (UDI) database. NeuroStructures, Inc. 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 NeuroStructures, Inc. manufacture?

NeuroStructures, Inc. specializes in orthopaedic and spinal fixation devices. Their product portfolio includes general internal orthopaedic fixation system implantation kits, spinal fixation plates made from non-bioabsorbable materials, polymeric spinal interbody fusion cages, and bone-screw internal spinal fixation systems that are non-sterile. They also produce reusable positioning instruments for orthopaedic prosthesis implantation, designed to assist surgeons during surgical procedures.

Where is NeuroStructures, Inc. based?

NeuroStructures, Inc. is headquartered in the United States. The company’s location is relevant for understanding its regulatory framework, as it operates under U.S. medical device regulations.

Which regulatory registries list NeuroStructures, Inc.’s devices?

NeuroStructures, Inc.’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry is used to track and identify medical devices in the U.S. market, ensuring traceability and compliance with regulatory requirements.

How are NeuroStructures, Inc.’s devices classified under U.S. regulations?

NeuroStructures, Inc.’s devices fall under Class II classification according to FDA regulations. This classification is typically assigned to devices that pose moderate risk and require special controls to ensure their safety and effectiveness, such as spinal fixation systems and orthopaedic implants.

What distinguishes NeuroStructures, Inc.’s spinal fixation devices from others in the market?

NeuroStructures, Inc. focuses on non-bioabsorbable spinal fixation plates, polymeric interbody fusion cages, and non-sterile bone-screw systems, which are designed for spinal stabilization. Their devices often include reusable positioning instruments for precision during orthopaedic surgeries, catering to both spinal and general orthopaedic fixation needs with a focus on durability and surgical efficiency.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
US
Address
—
LinkedIn
—
Facebook
—
Phone
8003526103
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
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DUNS Number
079391677

Catalogue (718)

Page 1 of 15
DeviceModel / ReferenceRegistriesClassStatus
Palladian™ 50-06-4525
FDA UDI
Class IIActive
Cavetto 100018-16188
FDA UDI
Class IIActive
Cortina 100198-200909
FDA UDI
Class IIActive
Cavetto 100018-14164
FDA UDI
Class IIActive
Cavetto 30-90-006P-121404
FDA UDI
Class IIActive
Cabo™ 81-0120
FDA UDI
Class IIActive
Cabo™ 98-1014
FDA UDI
Class IIActive
Cavetto 100018-14169
FDA UDI
Class IIActive
Cabo™ 81-0480
FDA UDI
Class IIActive
Cavetto 100018-121410
FDA UDI
Class IIActive
Cabo™ 81-0112
FDA UDI
Class IIActive
Palladian™ 50-90-0032
FDA UDI
Class IIActive
Tempus™ 10-15-012
FDA UDI
Class IIActive
Cabo™ 81-1614
FDA UDI
Class IIActive
Cabo™ 81-0342
FDA UDI
Class IIActive
Belvedere™ 12-90-015
FDA UDI
Class IIActive
Palladian™ 50-01-5540
FDA UDI
Class IIActive
Cortina 100035-250907
FDA UDI
Class IIActive
Transom™ 11-90-009
FDA UDI
Class IIActive
Palladian™ 50-07-5550
FDA UDI
Class IIActive
Transom™ 11-03-057
FDA UDI
Class IIActive
Tempus™ 10-03-054
FDA UDI
Class IIActive
Cortina 31-90-006-31091404
FDA UDI
Class IIActive
Transom™ 11-90-003
FDA UDI
Class IIActive
Palladian™ 50-04-0003
FDA UDI
Class IIActive
Belvedere™ 12-05-045
FDA UDI
Class IIActive
Cortina 100035-200910
FDA UDI
Class IIActive
Palladian™ 50-90-0018-01
FDA UDI
Class IIActive
Cabo™ 81-1210
FDA UDI
Class IIActive
Palladian™ 50-06-4535
FDA UDI
Class IIActive
Cabo™ 98-1103
FDA UDI
Class IIActive
Transom™ 11-90-015-010
FDA UDI
Class IIActive
Tempus™ 10-01-022
FDA UDI
Class IIActive
Cavetto 30-90-006-121410
FDA UDI
Class IIActive
Palladian™ 50-03-0035
FDA UDI
Class IIActive
Tempus™ 10-90-025
FDA UDI
Class IIActive
Palladian™ 50-90-0018-02
FDA UDI
Class IIActive
Tempus™ 10-01-012
FDA UDI
Class IIActive
Cortina 31-90-006-25091100
FDA UDI
Class IIActive
Palladian™ 50-90-0042
FDA UDI
Class IIActive
Tempus™ 10-01-020
FDA UDI
Class IIActive
Cavetto 30-90-006-141607
FDA UDI
Class IIActive
Cortina 31-90-006-20091404
FDA UDI
Class IIActive
Cavetto 30-90-006-121407
FDA UDI
Class IIActive
Tempus™ 10-12-014
FDA UDI
Class IIActive
Tempus™ 10-90-014
FDA UDI
Class IIActive
Cavetto 30-90-002-141606
FDA UDI
Class IIActive
Cabo™ 81-0348
FDA UDI
Class IIActive
Cortina 31-90-006-25090900
FDA UDI
Class IIActive
Cavetto 30-90-006P-161805
FDA UDI
Class IIActive

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