About Applied Silicone Corporation

Applied Silicone was founded in 1987 to serve healthcare, medical and specialty silicone markets. Since 1999, our primary focus has been on critical applications for short and long term medical devices.  With a complete portfolio of high purity silicones, ASC can supply fluids, gels, adhesives, LSR’s, HCR’s , elastomer dispersions and lubricant coatings.  Manufacturing and Quality Systems are GMP-based and ISO 9001:2008 certified quality management system.

Production Technology/ Industry Commitment

When other suppliers of implantable silicones are unable or unwilling to serve your application, Applied Silicone Corporation may be the solution to your problem. Our unique ability to formulate silicones from basic ingredients allows us to serve the most demanding applications. We have never faltered in our commitment to the medical product industry.

Product Development Excellence

Key members of staff have decades of direct experience serving the medical products business.  Put our extensive knowledge on material selection, performance, testing, qualification and design validation to work for your needs.  Meeting customer expectations is our goal and custom formulation and specifications are a specialty.

Technical and Production Consultation

Our experienced staff is always available to support customers with state-of-the-art testing and processing techniques. Consulting services include product and process design support, forensic analysis and expert defense witness testimony.

Quality Control

Our ISO 9001:2008 Certified Quality Management System and document control system meet the quality control demands of our customers. Our products are 100% quality tested.

Product Testing and Regulatory Compliance

ASC products are designed to meet FDA and ISO 10993 biocompatibility guidelines.  Our data base includes extensive chemical, physical and biological testing, including lifetime rat bioassays, which are compiled into Compendium Summaries that are available on a fee basis.  Compendiums are supported by extensive Material Master File records submitted to the FDA and selected notified bodies for reference purposes.  In most cases, our customers are not required to perform redundant, time consuming and expensive physical and preclinical biological testing because we already have data acceptable to the FDA and foreign Health Ministries.  Our staff is qualified and ready to assist you with your CE mark, 510K, IDE, and PMA throughout the world.