Accelerate Your MedTech Roadmap with Sanmina

From Prototype to Global Production

Visit Sanmina at MD&M West Booth 2923 to lock in the technical rigor your 2026 roadmap depends on. We provide ISO 13485 and FDA-registered production for complex medical devices, including surgical robotics, diagnostic imaging, and high-volume disposables. Secure your 30-minute session on the calendars below to discuss your path from prototype to global scale.

  • Design + Engineering

  • Complex System Integration

  • High-Volume Automated Manufacturing

  • Repair + Refurbishment

Book a 30-Minute Technical Strategy Session

Paul  Hoshino

Paul Hoshino

VP Business Development, Medical

Schedule Appointment
Mark Rehder

Mark Rehder

Global Account Director

Schedule with Mark

Global Medical Manufacturing Centers of Excellence

Technical Rigor at Scale: ISO 13485 · MDSAP Certified · FDA Registered*

AMERICAS

USA
Alabama*
California*
New Hampshire
Texas*
Wisconsin

Mexico
Guadalajara*
Monterrey

EMEA

Finland
Hungary
Ireland*
Israel*
Sweden*

APAC

India*
Kunshan*
Malaysia*
Shenzhen
Singapore*

Medical Device Markets

DIAGNOSTIC IMAGING

DIAGNOSTIC IMAGING

Ultrasound
MRI, CT, X-ray
Molecular Imaging

DIABETES CARE

DIABETES CARE

Blood Glucose Meters
Disposable Insulin Pumps
Continuous Glucose Monitors

IN-VITRO DIAGNOSTICS

IN-VITRO DIAGNOSTICS

Laboratory
Point-of-Care
Rapid Diagnostic

PATIENT MONITORING

PATIENT MONITORING

ECG/EKG, Pulse Oximeters
Hospital Vital Signs Monitors
Remote Patient Monitoring

ROBOTIC SURGERY

ROBOTIC SURGERY

Orthopedic
Minimally Invasive
Camera and Navigation Systems

BLOOD MANAGEMENT

BLOOD MANAGEMENT

Transfusion
Hemodialysis
Plasma Collection

CARDIOVASCULAR CARE

CARDIOVASCULAR CARE

Cardiac Monitors
Pulsed Field Ablation
Pacemaker, ICD, CRT

RESPIRATORY CARE

RESPIRATORY CARE

CPAP
Ventilators
Capnography

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