Modified Polymer Components
ISO 9001:2008 / ISO 13485:2003 Certified
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Precise Conformance Fully Documented

Our product development processes are fully documented from initial prototypes and pilot production to full-scale manufacturing.

Our staff conducts design reviews regularly to analyze every aspect of every project.

Modified Polymer Components uses Solid Works CAD software as the engineering and design and tool of choice. Our procedures support IQ, OQ and PQ documentation.

We are ISO 9001:2008 and
ISO 13485:2003 certified.


Uncompromised Quality

Modified Polymer Components expands the boundaries of what’s possible in medical device engineering, always maintaining high standards of excellence for manufacturing controls.

Modified Polymer ComponentsWe are capable of making many different very precise modifications to all types of polymer tubing, with company-wide, strictly adhered to quality control procedures in place each step of the way for assured, uncompromised quality you can rely on.

Incoming and Outgoing QC

We use Chatillon gauges and testers and other inspection tools to ensure thequality of incoming and outgoing products for our customers. Nearly all of our QC measurement devices are calibrated by an independent, outside source.

A lot history card is established at incoming QC. Items cited as non-conforming to lot history go to the Material Review Board (MRB) cage for examination. Final QC is staffed by one quality manager, one quality engineer, one senior inspector and five inspectors.

High Standards, Outstanding Results

Through ongoing efforts in research and continuing education, our staff maintains the highest level of skills, knowledge and professionalism found anywhere in the industry.

Medical device OEMs are invited to call Modified Polymer Components for consultation on product development and improvement, prototyping and manufacturing of polymer components.