Where patient-matched reconstruction makes the difference.
From severe traumatic brain injury decompressive craniectomy to aesthetic craniomaxillofacial (CMF) reconstruction, our implants are designed to address the indications where standard solutions have failed patients the most.
Cranial defect repair & reconstruction.
Class III indication for the Patient-Matched Skull Reconstruction System (Models DLZ04, DLZ05).
Severe TBI + decompressive craniectomy
Young 20–50 yr, 70% male. Large, irregular defects — often bifrontal. High infection risk with conventional mesh.
Ischaemic stroke + DC
Mid 50–70 yr. Hemispheric, large-area defects. The patient-matched geometry reduces operative time.
Aneurysm rupture
40–70 yr. Large, irregular defects. Multi-disciplinary team approach.
Brain tumour resection
40–70 yr. Often orbito-frontal or temporal defects. Aesthetic outcome matters.
Congenital deformity
0–10 yr. Dedicated paediatric sizes. Growing-skeleton considerations.
Paediatric trauma
5–18 yr. Paediatric size range. Long-term biocompatibility matters more.
Aesthetic CMF
30–60 yr. Forehead and temporal contour restoration. Highest aesthetic expectations.
Reconstruction after prior cranioplasty failure
Re-operation cases with poor soft-tissue envelope or contaminated field. Patient-matched geometry simplifies the case.
Post-resection reconstruction
Oncological resection defects. Customised to match the resected volume.
Beyond the cranium. The same platform, broader reach.
The ME-Fab® platform is indication-agnostic. We are extending the same patient-matched architecture into the broader craniomaxillofacial space.
Orbital floor
Patient-matched reconstruction of orbital floor and rim defects from trauma or tumour resection.
PipelineZygoma & malar
Custom zygomatic reconstruction with biomimetic micro-architecture for soft-tissue support.
PipelineMandible
Patient-matched mandibular plates and segmental reconstruction. Coordinated with vascularised fibula flap when needed.
PipelineInterbody fusion. Engineered for bone ingrowth.
The same gradient porous micro-architecture, applied to cervical and thoracic interbody fusion.
Cervical interbody
Patient-matched cervical interbody cages with porous endplates for endplate-matched fusion.
PipelineThoracic interbody
Patient-matched thoracic cages with gradient porous structure for load-bearing fusion.
PipelineCustom complex
Patient-specific complex spinal reconstruction for severe deformity or tumour cases.
PipelinePelvis. Acetabulum. Long bone.
High-complexity, low-volume trauma reconstruction where patient-matched geometry solves the case.
Pelvic & acetabular
Patient-matched reconstruction for complex acetabular fractures and pelvic discontinuity.
PipelineLong bone non-union
Custom plates and scaffolds for revision surgery of long-bone non-union.
PipelineOncological resection
Patient-matched endoprostheses for limb-salvage surgery after tumour resection.
PipelineOne-off. One-of-a-kind. Made to order.
For cases that don't fit any product family, our team works directly with the surgeon on a custom-made device pathway.
Custom-made devices
Under MDR Article 52(4) and the equivalent regulations in other jurisdictions, we can deliver patient-specific implants for unique clinical situations. The custom-made device pathway is the most flexible regulatory route for one-off complex reconstructions.
- Patient-specific complex reconstruction (e.g., post-trauma, post-oncology, congenital)
- Imaging-based design, surgeon-engineer sign-off, full quality release testing
- Regulatory pathway: custom-made device (EU MDR Art. 52(4)) or equivalent
- Lead time: project-dependent, typically 4–8 weeks
Have a complex case?
Our clinical engineering team works directly with surgeons on complex and custom reconstructions. Tell us about your case.