Patient Specific Implants

SU-POR® Patient-Specific Implants are individualized to match each patient’s unique anatomy and surgical needs. Designed in collaboration with the patient’s surgeon, these implants ensure a precise fit, optimal function, and aesthetic restoration.

Your Design, Crafted and Delivered with Precision

Expert Planning

Complementary planning session with our engineering team.

Risk Reduction

Sterilized in-house via Ethylene Oxide, reducing hospital liability and resources

Fast Delivery

Is shipped in as little as 8 business days, following Design Approval and Purchase Order

Complete Kit

Sterile implant(s), non-sterile medical model, and non-sterile sample for patient consultation

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CT Scan
Complete Digital Design Input Form
Upload Data and Files
CT Data Received
Utilize Preferred CT Scanning Protocol.
Complete Your Digital Design Input Form
Upload CT Data & Digital Design
CT Data Received

Once your CT data has been received, we will design a Patient-Specific Implant that will meet the functional and anatomic needs of the patient and surgeon. A graphic design proposal will be emailed for approval prior to manufacturing of the implant.

Our Key Features

Precises Fit

Each device is individually crafted to your patient’s specific needs.

Proven Material

Poriferous polyethylene, a biocompatible material with over 30 years of proven clinical performance.

Fast Turnaround

Order shipment in as little 8 business days following design approval.

Modification

Malleable, with Retained Shape Memory™ technology. SU-POR® implants allow for easy intraoperative modification with a scalpel blade, scissors, or burring instrument.

Variable Thickness


Variable thickness to match native bone. This ensures the implant matches the patient for premium results.

Virtual Approval Process

Detailed electronic document allows for approval prior to manufacturing, giving our engineers the tools they need to provide the highest quality results.

EO Sterile, Non-pyrogenic

Implant kit contains sterile, non-pyrogenic implant(s), limiting processing risk for the hospital.

MR Safe

This designation by the US FDA provides assurance of no image artifact or distortion of diagnostic MRI imaging.

Suture & Drainage

Sutures may be passed through any part of the implant. Open pores may allow drainage.

Tissue In-Growth

The interconnecting, omnidirectional pore structure allows for fibrovascular and tissue integration, giving the implant its own blood supply.

Application

To meet the need of individual patients in applications of craniofacial reconstructive/cosmetic surgery and repair of craniofacial trauma.

Direct Fixation

Screws may be inserted directly through the implant margins into the bone and may eliminate the need for plate fixation.