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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 2 of 3
DeviceModel / ReferenceRegistriesClassStatus
Revolution 1164550C
FDA UDI
Class IIActive
Mediant Anterior Cervical Plate 1214010
FDA UDI
Class IIActive
Mediant Anterior Cervical Plate 12102043
FDA UDI
Class IIActive
Revolution Spinal System 1164530TL
FDA UDI
Class IIActive
Revolution 11665304
FDA UDI
Class IIActive
Revolution 1163035C
FDA UDI
Class IIActive
Revolution Spinal System 1163035UC
FDA UDI
Class IIActive
Revolution Spinal System 1162530TLC
FDA UDI
Class IIActive
Mediant Anterior Cervical Plate 12101024
FDA UDI
Class IIActive
Mediant 121308
FDA UDI
Class IIActive
Mediant Anterior Cervical Plate 12103078
FDA UDI
Class IIActive
Revolution 11645454
FDA UDI
Class IIActive
Revolution 11675254
FDA UDI
Class IIActive
Revolution 11665554
FDA UDI
Class IIActive
Revolution Spinal System 1162530XC
FDA UDI
Class IIActive
Revolution 11665254
FDA UDI
Class IIActive
Mediant Anterior Cervical Plate 1214514
FDA UDI
Class IIActive
Revolution Spinal System 1161520UC
FDA UDI
Class IIActive
Mediant Anterior Cervical Plate 12102046
FDA UDI
Class IIActive
Revolution Spinal System 1165540TL
FDA UDI
Class IIActive
Mediant Anterior Cervical Plate 12103075
FDA UDI
Class IIActive
Revolution Spinal System 1167540TL
FDA UDI
Class IIActive
Mediant Anterior Cervical Plate 1214016
FDA UDI
Class IIActive
Mediant Anterior Cervical Plate 1214512
FDA UDI
Class IIActive
Revolution 11675354
FDA UDI
Class IIActive
Mediant Anterior Cervical Plate 1214012
FDA UDI
Class IIActive
Revolution 11655254
FDA UDI
Class IIActive
Revolution 11665354
FDA UDI
Class IIActive
Revolution 1165055C
FDA UDI
Class IIActive
Mediant Anterior Cervical Plate 12103057
FDA UDI
Class IIActive
Revolution 11665504
FDA UDI
Class IIActive
Mediant Anterior Cervical Plate 12102049
FDA UDI
Class IIActive
Revolution 11655404
FDA UDI
Class IIActive
Revolution 11675554
FDA UDI
Class IIActive
Mediant Anterior Cervical Plate 12101022
FDA UDI
Class IIActive
Revolution 11645304
FDA UDI
Class IIActive
Revolution Spinal System 1164535TL
FDA UDI
Class IIActive
Mediant Anterior Cervical Plate 12102040
FDA UDI
Class IIActive
Revolution 1161520C
FDA UDI
Class IIActive
Revolution Spinal System 1162025UC
FDA UDI
Class IIActive
Revolution 11675504
FDA UDI
Class IIActive
Revolution Spinal System 1167555TL
FDA UDI
Class IIActive
Revolution Spinal System 1164550TLC
FDA UDI
Class IIActive
Revolution Spinal System 1167525TL
FDA UDI
Class IIActive
Revolution 11645504
FDA UDI
Class IIActive
Revolution Spinal System 1162025TLC
FDA UDI
Class IIActive
Mediant Anterior Cervical Plate 12101028
FDA UDI
Class IIActive
Revolution 11675404
FDA UDI
Class IIActive
Revolution 11675454
FDA UDI
Class IIActive
Revolution Spinal System 1166555TL
FDA UDI
Class IIActive

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