At Greyack medical Co., Ltd, our leadership team is dedicated to building long-term, collaborative partnerships with global medical device Original Equipment Manufacturers (OEMs). We integrate seamlessly into your device development pipeline, ensuring that every design for manufacturability (DFM) review, prototype iteration, and production run exceeds stringent international quality requirements.
Driven by an engineering mindset and entrepreneurial agility, our executive directors maintain a steadfast commitment to zero-defect quality, on-time global delivery, and transparent regulatory traceability.
FDA Registration: Fully registered facilities operating under 21 CFR Part 820 Quality System Regulations (QSR).
ISO 13485:2016 Certified: Rigorous quality management systems certified for orthopedic implants, surgical robotics, and life-science tools.
Engineering Leadership: Over two decades of hands-on expertise in multi-axis Swiss CNC turning, micro-grinding, and 3D additive manufacturing.
Combining specialized manufacturing knowledge with enterprise-grade operational standards across our production facilities.
Our management team includes veteran manufacturing engineers, quality managers, and medical industry experts. Their technical background guarantees that technical drawings, geometric dimensioning and tolerancing (GD&T), and material certifications are reviewed with extreme precision.
We foster an enterprise-wide culture of continuous improvement and knowledge sharing. By unifying best practices in multi-axis CNC machining, titanium passivation, and cleanroom packaging, Greyack medical Co., Ltd delivers scalable production solutions for complex surgical instruments.
Guided by proactive executive planning, Greyack medical Co., Ltd continually invests in state-of-the-art machinery, automated robotic cells, laser metrology, and powder-bed fusion 3D metal printing platforms to support next-generation medical device innovation.
From initial risk analysis and prototype validation to commercial high-volume manufacturing, Greyack medical Co., Ltd leaders oversee every step of supply chain execution. Our cross-functional teams work collaboratively with OEM procurement directors, quality engineers, and regulatory officers.
By pairing lean manufacturing protocols with robust Design History File (DHF) and Device Master Record (DMR) documentation, we streamline regulatory submissions and shorten time-to-market for complex medical programs.
Discover how Greyack medical Co., Ltd leadership and technical capabilities can support your surgical implant, instrument, or robotics program. Send your technical drawings and specifications directly to our engineering team at [email protected].
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