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Vistek Procedure Validations Ensure Compliance

Wade Phillips
Director of Business Development
937-694-0081

Vistek Medical Completes Process Validations, Expands Capacity

Vistek Medical, a Pennsylvania based ISO 13485 certified medical device contract manufacturer, announced today the successful completion of its Process Validations, allowing the company to now offer validated services in cleaning, passivation, electro polishing, anodizing and laser etching. In addition, Vistek has significantly expanded its business capacity, allowing the company to increase full-scale production and offer rapid response solutions to customers.

“Coming off of a record sales year, we felt this was a perfect time to grow our business model,” said Vincent Visco, President of Vistek. “We have purchased five additional CNC machines and added several employees to expand our capacity to support orthopedic surgical teams, and do it well. In addition, we are excited that our precision processes have been validated by an independent lab.”

Vistek offers a full range of contract manufacturing capabilities for the spinal, trauma, extremity, and sports medicine medical device needs of clients and developers world-wide.

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