PoreStarA new class of implant material
PoreStar (porous polyethylene) surgical implants are individually designed from 3D CT scans to get the best possible patient outcome: plan your reconstruction and design your implants. PoreStar implants are indicated for the repair or augmentation of craniofacial bone including defects caused by trauma, tumour or a congenital disorder. This includes augmentation or restoration of contour in the craniofacial skeleton and cranioplasties. PoreStar is manufactured from porous high density polyethylene (HDPE).
PoreStar Surgical Implants
Manufactured from a star to creates a unique bone-like porous architecture
Porosity may permit hard and soft tissue adhesion to secure the implant
Surgeon can perform minor modifications with a scalpel and shape or feather the edges of the implant after fixation
CT and MRI compatible; radiolucent and non-magnetic for compatibility with post-operative imaging
Supplied with a BioModel (anatomical replica) with every case
Porous Polyethylene - Proven Clinical History
Clinical history of reconstruction and augmentation in the maxillofacial region1
Tissue ingrowth stabilises the surgical implant2
The biocompatibility standard based on long term stability and virtual lack of inflammatory response3
Design Your Implant
Surgeon can contribute to the implant design or decide on tumour resection margins
Online implant design review service available via AnatomicsC3D
BioModel and implant prototype can be sent to the surgeon for review with the patient as part of the design process
- Menderes A., et al. Craniofacial reconstruction with high-density porous polyethylene implants. J Craniofac Surg. 2004 Sep;15(5):719-24.
- Park HK., et al. Biomechanical properties of high-density polyethylene for pterional prosthesis. Neurol Res. 2002 Oct;24(7):671-6.
- Lacey M., et al. Use of porous high-density polyethylene implants in temporal contour reconstruction. J Craniofac Surg.1993 Apr;4(2):74-8. J Craniofac Surg. 1993 Apr;4(2):74-8.