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Oral maxillofacial surgery


MEDPOR has been a trusted name in the industry since 1985, with hundreds of thousands of procedures performed, and hundreds of published clinical reports in reconstructive, cranial, oculoplastic, and cosmetic applications.

Our MEDPOR product line provides you an array of porous polyethylene solutions for your reconstruction and augmentation needs. We understand that bio-compatibility characteristics of implants are paramount to help surgeons achieve positive patient outcomes. The omni-directional pore structure of our polyethylene implants may increase implant acceptance by allowing the patient‘s native tissue to integrate with the implant. In addition to our comprehensive line of stock MEDPOR implants, we offer CT-based patient-specific implants, putting the implant design in your hands.

Proven. Adaptable. Comprehensive.

MEDPOR TITAN Double Barrier BTBMEDPOR Titan Double Barrier BTB

MEDPOR Orbital Floor and Wall MTB LeftMEDPOR Orbital Floor and Wall MTB Left

MEDPOR TITAN 3D Orbital Floor - LargeMEDPOR TITAN 3D Orbital Floor - Large

MEDPOR TITAN 3D Orbital Floor - SmallMEDPOR TITAN 3D Orbital Floor - Small


Features and benefits

30 years of proven clinical history

Proven material

More than 400,000 procedures have been performed with MEDPOR Biomaterial, with more than 350 published clinical reports in cranial, reconstructive, oculoplastic and cosmetic applications.

Comprehensive portfolio

The MEDPOR Orbital product line consists of implants to fit individual patient needs.

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If desired, MEDPOR material may be cut and shaped to fit patient and surgeon needs.


Implants packaged sterile and ready to use. They can be stored in the hospital or office to have on hand as needed.

MEDPOR Orbital Floor and Wall MTB Left


Combines high-density polyethylene sheets and titanium mesh in a single implant for increased flexibility, shape retention, radiographic visualization and strength.1

Clinical evidence

To determine the safety and efficacy of using porous high-density polyethylene (PHDPE) in the repair of orbital defects.

Retrospective case series.

Academic tertiary care trauma center. Patients One hundred seventy patients with orbital defects requiring surgical repair. Intervention Orbital defect repair with PHDPE. Main Outcome Measure Our review documents surgical results and complications associated with the use of PHDPE.

There was a 6.4% complication rate associated with the use of PHDPE. The infection rate was 1.8%. The persistent orbital malposition rate was 3.5%. The extrusion rate was 0%.

This report represents the largest case series in the literature using PHDPE for orbital reconstructions. The use of PHDPE resulted in a low complication rate and excellent functional and cosmetic reconstructive results. Because of our success with the use of PHDPE, we have changed our clinical practice to minimize the use of autologous graft material, thereby eliminating donor site morbidity in cases involving orbital reconstruction.

Full Article

To evaluate our initial experience with a porous polyethylene implant with embedded titanium in orbital reconstruction.

A retrospective review of the charts was performed for patients receiving at least 1 orbital porous polyethylene implant with embedded titanium from October 2004 through April 2006. Patient demographics, implant type and size, method of fixation, postoperative complications, and length of follow-up were recorded.

One-hundred six patients received at least one embedded titanium implant (80 men, 26 women). Age ranged from 3 years to 85 years (mean, 31 years). Indications included orbital fracture repair (102 patients), correction of enophthalmos (3 patients), and reconstruction after tumor resection (1 patient). The average floor implant used was 22.3 mm wide by 27.9 mm long. The average medial wall implant was 13.6 mm tall by 22 mm long. Implants were fixated with 1 or 2 microscrews in 75 patients (70.8%) and placed without fixation in 31 patients (29.2%). Four postoperative complications were noted: a retrobulbar hemorrhage on postoperative day 3 that resolved without sequelae, a vertical overcorrection requiring removal of the implant, a transient oculomotor disturbance, and a screw placed in proximity to the infraorbital nerve canal resulting in hypesthesia and chronic pain that required removal of the screw. In the 3 complications potentially related to the implant, the embedded titanium allowed postoperative implant visualization and guided subsequent management. No implant extrusions or postoperative infections were noted.

Porous polyethylene implants with embedded titanium provide a new alternative to alloplastic implant materials for orbital reconstruction with a profile that combines several advantages of porous polyethylene and titanium implants.

Full Article


1: Holck, D., Foster J., and Dahl T., “Custom Shaped Porous Polyethylene-Titanium Mesh Orbital Implants for Internal Orbital Floor/Medial- Wall Fracture Repair” ASOPRS 37th Annual Fall Scientific Syllabus, pp190, November 15-16, 2006

CMF-WC-54_Rev. None_18993


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