Pro-dex

Staying Ahead of the Curve

The development of powered surgical devices requires extreme focus on protecting critical components from harsh environments such as vacuum autoclaves, high pH cleaning solutions, or saline. Pro-Dex follows a six-phase development process that helps address these challenges.

With only one goal in mind - product excellence - the six-phase development process consists of:

Throughout, the Pro-Dex Quality Management System (QMS) continually assesses and documents key compliance characteristics. Each product is then reviewed and rigorously tested to ensure that all electrical safety, biocompatibility, sterilization validation, and appropriate shelf-life standards/requirements are met.

Pro-Dex stays ahead of the curve by continually evolving and adapting the design process in an effort to meet the constantly changing ISO and FDA guidelines. This process is supported by a comprehensive documentation system that consists of project planning timelines, design element checklists, project phase design reviews, verification and validation test plans, as well as a complete and compliant design history file.

Markets and Application Pro-Dex has Served

• Medical
  
  • Arthroscopy handpieces
  • Cranial-maxillofacial handpieces
  • Spinal
  • Orthopedic
  • Electric
  • Battery-powered
  • Pneumatic
• Dental
  
  • High-speed rotary system
  • Low-speed rotary system
  • Prophy
  • Electric
  • Battery-powered
  • Pneumatic
• Industrial
  
  • Air motors