Patient-Matched · Additive Manufacturing · Regenerative

The world's first clinically validated, patient-matched titanium cranial implant.

Excellent MedTech pioneers personalised 3D-printed titanium reconstruction and regenerative medicine — bridging the gap from form to function to regeneration.

< 2%Total complication rate
5,000+Clinical cases delivered
60+Patents & IP rights
NMPAClass III approved
Technology in Motion

From a CT scan to a living implant.

Six animations, one pipeline. Every stage of patient-matched implant manufacturing — captured as it actually happens on the production floor.

01 · EBM Build
60 kV · < 10⁻³ mbar · 700°C

Electron Beam Melting

Layer-by-layer build of Ti-6Al-4V ELI in vacuum. 50–100 µm layer thickness, 60 kV electron beam, 700 °C pre-heat.

02 · Micro-Architecture
porosity 60–80% 300–800µm gradient

Gradient Porous Micro-Architecture

60–80% porosity in the bone-contact zone, 20–40% in the load-bearing zone. 300–800 µm pore size for vascularised bone ingrowth.

03 · Patient Pipeline
CT DESIGN EBM 5–7 working days · ±10% backup · DHL/FedEx

CT → Design → EBM → Surgery

One pipeline. Five working days. The patient sends a CT scan; we return a sterile, ready-to-implant personalised prosthesis.

04 · Osseointegration
TiO₂ · Ti-OH vascularised bone ingrowth

Bone Ingrowth at the Interface

Native TiO₂ chemistry · Ti-OH groups · protein adsorption · osteoblast adhesion · vascularised bone ingrowth through interconnected pores.

05 · 100% Inspection
100% PASS vs. design STL

100% CMM Inspection

Every implant is CMM-inspected to ISO 10360 and CT-scanned against its design STL. Zero-defect release criterion.

06 · Sterile Delivery
EO STERILE · ISO 11135 · ISO 11607

EO Sterilised, Double-Pouched

ISO 11607 double-pouch in ISO Class 7 cleanroom. EO sterilisation per ISO 11135. Validated 5-year shelf life. DHL / FedEx direct to hospital.

Trusted by 500+ hospitals & clinical partners
Why Excellent MedTech

From "fill the hole" to "regenerate the bone".

Three generations of implant technology, one patient. We deliver anatomical match, biomechanical strength, and a long-term pathway to regeneration — the first PSI implant validated by a large-cohort prospective clinical study.

01 · Form

Perfect anatomical match

CT/MRI 3D reconstruction plus biomimetic dual-surface design restores natural cranial curvature 1-to-1 — sub-millimetre accuracy on first placement.

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02 · Function

Outstanding mechanical & biological performance

Ti-6Al-4V ELI with gradient-optimised porous micro-architecture. 1,400 N compressive strength, ≥ 5 million cycle fatigue, native TiO₂ osseointegration.

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03 · Regeneration

A platform built for the future of tissue repair

Beyond reconstruction: protein-engineering (ME-Regen®) and tissue engineering (Cell home®) extend the same platform into in-situ regeneration.

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0+Clinical cases delivered
0+Hospital partners
0+Patents & IP rights
0Invention patents granted
Clinical Evidence

The data that changes the conversation.

In head-to-head literature comparisons, our patient-matched implants deliver total complication rates one-fifth of conventional mesh and one-tenth of PEEK plates.

Total complication rate

Excellent MedTech 3D PSI< 2%
Titanium mesh (literature)12.2–17.4%
PEEK plate (literature)17.2–18.5%

Source: large-cohort prospective clinical study vs. peer-reviewed literature controls.

Infection rate

Excellent MedTech 3D PSI< 1.7%
Titanium mesh (literature)6.05–8.2%
PEEK plate (literature)5.1–8.8%

Lower infection = fewer re-operations, less antibiotic exposure, lower total cost of care.

Re-operation (critical failure)

Excellent MedTech 3D PSINone observed
Titanium mesh (literature)3.70%
PEEK plate (literature)8.60%

Validated across 5,000+ implants delivered to date.

Three Technology Platforms

A single R&D engine. Three revolutions in patient care.

Our research institute operates three integrated platforms — each addressing a different layer of the human tissue repair problem.

ME-Fab®

Additive manufacturing of personalised implants

From 30,000+ clinical cases, our deep-learning models achieve 95%+ bionic match — and ship it as a Class III implant.

  • Electron Beam Melting of Ti-6Al-4V ELI
  • Gradient-optimised porous micro-architecture
  • Patient-specific 1:1 anatomical reconstruction
  • Validated for cranial, maxillofacial, orthopaedic
Explore ME-Fab® →
ME-Regen®

Nobel-grade controlled release for in-situ regeneration

Microgram-level precision protein delivery extends therapeutic retention to 2–4 weeks — the holy grail of regenerative pharmacology.

  • Low-dose, long-acting protein release
  • Tunable release kinetics
  • Bone, skin, vascular, neural applications
  • Closed-loop R&D; pilot & clinical coming
Explore ME-Regen® →
Cell home®

In-vivo tissue engineering & organ transplant

Beyond repair: building consistent, functional human tissue for transplant — solving donor ethics and shortage in one stroke.

  • In-vitro and in-vivo tissue manufacturing
  • Bone, cartilage, skin, vascular, neural
  • Eliminate donor-site morbidity
  • Pilot scale; clinical coming
Explore Cell home® →
From CT to Surgery

Five stages. Five to seven working days.

You send the CT. We return a sterile, ready-to-implant patient-matched prosthesis. Lead time 5–7 working days (3 days expedited).

1

Clinical Intake

Surgeon sends DICOM + defect description. Medical engineer responds within 24 h.

2

Image & Design

3D reconstruction → biomimetic design → gradient optimisation → FEA validation.

3

Medicine-Engineering Interaction

Surgeon & engineer sign off on the design — no intra-operative "discovery".

4

Precision Manufacturing

Electron Beam Melting, post-processing, 100% CMM inspection, double-pouch sterile pack.

5

Direct Logistics

DHL / FedEx to hospital. ±10% backup implant shipped together.

Featured Product

Additive Manufacturing Patient-Matched Skull Reconstruction System

Class III implant system designed for cranial defect repair and reconstruction. Models DLZ04 & DLZ05. Size range 30–200 mm. Made of medical-grade Ti-6Al-4V ELI titanium alloy, manufactured by Electron Beam Melting.

  • Biomimetic dual-surface: porous for bone ingrowth, smooth for soft tissue
  • 1,400 N compressive strength · 5×10⁶ cycle fatigue
  • 1:1 patient-specific geometry from CT / MRI DICOM
  • CT-clear imaging · MRI-safe · Non-magnetic
MODEL DLZ04 / DLZ05
MaterialTi-6Al-4V ELI
Size range30–200 mm
ProcessElectron Beam Melting
ClassNMPA Class III
Cert. No.国械注准 20263130176
Lead time5–7 working days
Global Reach

Engineered in Shenzhen. Available in 40+ countries.

From Tier-1 Chinese academic hospitals to leading European neurosurgical centres, our patient-matched implants are designed to meet the most stringent international standards.

CHINA
Tier-1 academic hospitals

Beijing Tiantan, Huashan, Xuanwu, FMMU, Southern Medical, Shenzhen Second People's.

EUROPE
CE-MDR in progress

Charité Berlin, MHH Hannover, LMU Munich, AP-HP Paris, Niguarda, Vall d'Hebron.

U.S.
FDA 510(k) scoping

Engagement with FDA CDRH. Targeting Class II 882.5320 (GWO) or equivalent.

MDSAP
5 markets, 1 audit

Single audit for US, Canada, Australia, Japan, Brazil — in scoping.

Regulatory & Quality

Built to the highest global standard.

Our quality system is engineered for the world's most demanding medical device regulators — from NMPA Class III to CE-MDR and FDA 510(k).

Granted

NMPA Class III

国械注准 20263130176

Certified

ISO 13485

QMS for medical devices

Certified

GMP

Production of Class III devices

In progress

CE-MDR

Class III, Rule 8

Case Studies & Real Outcomes

5,000+ patients. Real stories. Real data.

Every implant we ship has a patient and a surgeon behind it. Here is what the workflow looks like in practice — and what the 6-month follow-up data says.

Featured Case · Clinical Trial

Large left temporoparietal skull defect

A 38-year-old male patient with severe TBI and decompressive craniectomy. Full CT-to-surgery workflow with 6-month follow-up.

  • Stage 1: Clinical intake — 24 h response
  • Stage 2: 3D reconstruction + biomimetic design + FEA
  • Stage 3: MEI sign-off with operating surgeon
  • Stage 4: EBM build + 100% CMM inspection
  • Stage 5: DHL/FedEx, ±10% backup, 5 working days

6-month follow-up outcomes

  • Implant integration: 100% — no loosening, migration, or exposure
  • Cranial symmetry: Restored 1:1 to natural curvature
  • Complications: None observed
  • Re-operation: None required
  • Foreign-body sensation / chronic headache: None
  • Surgeon assessment: "The MEI workflow changes the surgical experience."
View the full case library →
< 2% Total complication rate
0% Critical failure re-operation
5,000+ Patients across the dataset
50+ Clinical trial sites

Bring patient-matched reconstruction to your hospital.

Join 500+ clinical partners worldwide. Talk to our team about distribution, OEM/ODM, or co-development. We respond within 24 hours.