Collaboration With Surgeons

Combined the founders bring over 68 years of experience

If you’re a surgeon, device developer, or medical manufacturer seeking precision machining solutions, we’d love to talk. Our team responds within one business day.

At our ISO 13485–certified machining facility, we partner directly with surgeons to design, engineer, and manufacture high-quality medical implants, surgical instruments, and custom procedural tools. Our goal is to turn clinical insight into reliable, manufacturable solutions that improve patient care.

We work closely with surgeons to translate conceptual ideas and clinical needs into fully engineered designs.

  • Early-stage concept development
  • Design-for-manufacturability (DFM) guidance
  • CAD modeling & rapid revisions
  • Prototype-to-production transition

We specialize in precision machining of complex implant geometries and patient-specific designs.

  • Titanium, stainless steel, cobalt-chrome
  • Custom plates, screws, spacers, cages, and fixation systems
  • Tight-tolerance life-critical components

From single-use to reusable instruments, we support the full development cycle.

  • Cutting, gripping, manipulation, and positioning tools
  • Ergonomic design improvements based on surgeon feedback
  • High-performance materials suited for sterilization

Fast turnaround for prototypes enables surgeons to evaluate fit, function, and ergonomics early in the process.

  • Machined prototypes
  • Iterative testing
  • Pilot production runs

Our ISO 13485–compliant processes ensure repeatability and product quality.

  • CNC milling, turning, and micro-machining
  • Full traceability and documentation
  • Quality control with advanced inspection
  1. Discovery Meeting – Discuss your clinical challenge or device idea
  2. Design Phase – CAD development and design refinement
  3. Prototype Production – Functional prototypes for review
  4. Testing & Iteration – Adjustments based on surgeon feedback
  5. Final Manufacturing – Scalable production with strict QA
  • ISO 13485–certified facility
  • Experience with medical device standards & regulatory expectations
  • Fast, agile development
  • Ability to manufacture both custom and production-scale devices
  • Direct communication with engineers and machinists