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Company Overview

A global leader in personalised human tissue repair.

Shenzhen Excellent Technology Co., Ltd. (Excellent MedTech) is a pioneer in patient-matched 3D-printed titanium reconstruction and regenerative medicine. Founded to address the largest unmet needs in skeletal and soft-tissue repair, we have grown from a single-product company into a three-platform regenerative medicine enterprise.

Our Mission

Restore form. Restore function. Restore the future of tissue regeneration.

Every implant we ship is engineered to do three things: match the patient's anatomy 1-to-1, withstand decades of physiological load, and serve as a platform for the next generation of regenerative therapies. We exist to close the gap between what standard implants can do and what each patient actually needs.

The human skeletal system is the most architecturally complex structure in the body. Treating it requires more than off-the-shelf plates and screws. It requires a complete patient-data-to-implant pipeline that respects the individuality of every fracture, defect, and surgeon.

2014Founded
ShenzhenHeadquarters
5,000+Cases delivered
500+Hospital partners
60+IP rights
800 m²Smart factory + 5,000 m² expansion
Our Story

From a single implant to a three-platform regenerative enterprise.

2014 — Foundation
Shenzhen Excellent Technology Co., Ltd. established

Founded with a singular focus: personalised human skeletal repair through additive manufacturing. Core team brings together biomedical engineering, clinical medicine, and materials science.

2016 — First clinical cases
First patient-matched cranial implants shipped

Early clinical collaborations with the Fourth Military Medical University and Southern Medical University affiliated hospitals validate the technology in a real-world setting.

2018 — 100 case milestone
First large-cohort clinical dataset

By 2018, the dataset reaches 100+ cases — and the complication rate is already in the low single digits, confirming the original hypothesis.

2020 — IP moat
60+ IP rights; Guangdong Provincial Science & Technology Award

Recognised by the Guangdong Provincial Government with the Science and Technology Invention Award (Second Prize) for core technical innovation.

2022 — Multi-platform
ME-Fab®, ME-Regen®, Cell home® consolidated

Three integrated R&D platforms — additive manufacturing, protein engineering, tissue engineering — form the basis of the long-term regenerative strategy.

2023 — Quality system
GMP and ISO 13485 dual certification

Quality system certified for the production of Class III medical devices. Lay the foundation for international regulatory submissions.

2024 — Scale
800 m² smart factory + 5,000 m² expansion plan

First GMP factory operational; 5,000 m² modern additive manufacturing and biomanufacturing centre in planning to meet global demand.

2026 — Global expansion
NMPA Class III + CE-MDR + FDA + MDSAP in motion

International expansion: regulatory submissions in EU, US, UK, Canada, Australia, Japan, and Brazil. KOL network activated across EANS, AOCMF, EuroCMF.

Core Values

Technology-driven. Standards-led. Market-validated. Team-excellent.

Technology-driven

Three proprietary R&D platforms and 60+ IP rights form an integrated technology engine.

Standards-led

Co-author of 10 national guidelines, 2 expert consensuses, and 2 group standards — shaping the industry.

Market-validated

5,000+ cases across 500+ hospitals. 3 months to obtain reimbursement coding. 1 month for multi-province pricing.

Team excellent

Cross-disciplinary team with national and provincial-level awards, including National Science & Technology Progress Award winners.

By the Numbers

Excellence in every dimension.

0+Clinical cases
0+Hospital partners
0+IP rights
0Invention patents
Where We Operate

Headquartered in Shenzhen. Active worldwide.

Shenzhen, China Headquarters & Manufacturing
  • 10B Kechuang Building, Quanzhi Tech Innovation Park, Bao'an District
  • Shenzhen Center for Advanced Additive Manufacturing & Biomanufacturing
  • 800 m² operational + 5,000 m² expansion in planning
Europe Regulatory & clinical engagement
  • CE-MDR Class III in progress (TÜV SÜD / DEKRA target)
  • KOL network: Charité, MHH, LMU, AP-HP, Niguarda, Vall d'Hebron
  • Engagement: EANS · AOCMF · EuroCMF
United States Regulatory & distribution scoping
  • FDA 510(k) pathway scoping (CDRH)
  • Engagement: AANS · CNS · NREF · AAOMS
  • Distribution: GPOs and academic hospital channels

Want to know more?

Read about our leadership team, manufacturing facility, or the history behind Excellent MedTech.

Leadership Team Manufacturing Facility