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INTELLIGENT IMPLANT SYSTEMS, LLC

US

Last updated May 27, 2026

What INTELLIGENT IMPLANT SYSTEMS, LLC makes

Intelligent Implant Systems, LLC produces sterile bone-screw internal spinal fixation systems designed for spinal stabilization, including anterior cervical plates for cervical spine surgery. Their portfolio also includes non-bioabsorbable spinal fixation plates intended for internal fixation of spinal segments.

These devices are classified as Class II under FDA regulations and are authorised through the 510(k) and UDI pathways. The company is based in the United States and its products are listed in the FDA’s regulatory databases.

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 Intelligent Implant Systems, LLC manufacture?

Intelligent Implant Systems, LLC specializes in spinal fixation devices, including sterile bone-screw internal spinal fixation systems and non-bioabsorbable spinal fixation plates. These products are primarily used for spinal stabilization, such as the Mediant Anterior Cervical Plate and the REVOLUTION SPINAL SYSTEM, which are designed for cervical spine surgery and internal fixation of spinal segments.

Where is Intelligent Implant Systems, LLC based?

The company is headquartered in the United States. This location aligns with its regulatory focus on FDA compliance for its spinal fixation devices.

Which regulatory registries list Intelligent Implant Systems, LLC’s devices?

Intelligent Implant Systems, LLC’s devices are listed in the FDA’s 510(k) and Unique Device Identifier (UDI) databases. These registries track devices authorised through the 510(k) pathway and ensure traceability via UDIs, which are required for Class II devices like those produced by the company.

How are Intelligent Implant Systems, LLC’s devices classified under FDA regulations?

The company’s devices, including bone-screw internal spinal fixation systems and non-bioabsorbable spinal fixation plates, fall under Class II classification by the FDA. This classification applies to devices that pose moderate risk and require special controls to ensure safety and effectiveness, such as premarket notifications (510(k)) and UDI compliance.

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

Information

Country
US
Address
—
LinkedIn
—
Facebook
—
Phone
704-424-1009
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
—
DUNS Number
013742030

Catalogue (124)

Page 1 of 3
DeviceModel / ReferenceRegistriesClassStatus
Mediant Anterior Cervical Plate 12101019
FDA UDI
Class IIActive
Revolution Spinal System 1162025XC
FDA UDI
Class IIActive
Mediant Anterior Cervical Plate 12101032
FDA UDI
Class IIActive
Revolution Spinal System 1165535TL
FDA UDI
Class IIActive
Revolution Spinal System 1166550TL
FDA UDI
Class IIActive
Mediant Anterior Cervical Plate 12101026
FDA UDI
Class IIActive
Revolution Spinal System 1165530TL
FDA UDI
Class IIActive
Revolution Spinal System 1166545TL
FDA UDI
Class IIActive
Revolution 11655304
FDA UDI
Class IIActive
Revolution 1161520S
FDA UDI
Class IIActive
Revolution 1164045C
FDA UDI
Class IIActive
Revolution 1163540C
FDA UDI
Class IIActive
Revolution 11645404
FDA UDI
Class IIActive
Revolution Spinal System 1165550TL
FDA UDI
Class IIActive
Revolution 11655554
FDA UDI
Class IIActive
Revolution Spinal System 1164525TL
FDA UDI
Class IIActive
Revolution Spinal System 1167530TL
FDA UDI
Class IIActive
Revolution 11665454
FDA UDI
Class IIActive
Mediant Anterior Cervical Plate 12103069
FDA UDI
Class IIActive
Revolution Spinal System 1165545TL
FDA UDI
Class IIActive
Revolution Spinal System 1164545TL
FDA UDI
Class IIActive
Revolution Spinal System 1166540TL
FDA UDI
Class IIActive
Mediant Anterior Cervical Plate 12102052
FDA UDI
Class IIActive
Revolution 1162530S
FDA UDI
Class IIActive
Revolution Spinal System 1163035TLC
FDA UDI
Class IIActive
Revolution Spinal System 1164045TLC
FDA UDI
Class IIActive
Mediant Anterior Cervical Plate 12101020
FDA UDI
Class IIActive
Revolution Spinal System 1161520XC
FDA UDI
Class IIActive
Revolution 11655354
FDA UDI
Class IIActive
Revolution 11645254
FDA UDI
Class IIActive
Mediant 121309
FDA UDI
Class IIActive
Mediant Anterior Cervical Plate 12103060
FDA UDI
Class IIActive
Revolution 11675304
FDA UDI
Class IIActive
Revolution Spinal System 1166535TL
FDA UDI
Class IIActive
Mediant Anterior Cervical Plate 12101030
FDA UDI
Class IIActive
Revolution 1162530C
FDA UDI
Class IIActive
Revolution 1162025C
FDA UDI
Class IIActive
Revolution Spinal System 1167535TL
FDA UDI
Class IIActive
Revolution Spinal System 1164540TL
FDA UDI
Class IIActive
Revolution 11665404
FDA UDI
Class IIActive
Mediant Anterior Cervical Plate 12101034
FDA UDI
Class IIActive
Revolution Spinal System 1167550TL
FDA UDI
Class IIActive
Mediant 121302
FDA UDI
Class IIActive
Mediant Anterior Cervical Plate 1214518
FDA UDI
Class IIActive
Revolution Spinal System 1163540TLC
FDA UDI
Class IIActive
Mediant Anterior Cervical Plate 1214516
FDA UDI
Class IIActive
Revolution Spinal System 1161520TLC
FDA UDI
Class IIActive
Mediant Anterior Cervical Plate 1214510
FDA UDI
Class IIActive
Revolution Spinal System 1166525TL
FDA UDI
Class IIActive
Revolution Spinal System 1164550TL
FDA UDI
Class IIActive

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