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OSAP 2018 Speaker Bio Steen



  Annual Conference Speakers

  Andrew I. Steen




   Speaker Bio

Mr. Andrew Steen is Reviewer/Mechanical Engineer for the Center for Device and Radiological Health/Office of Device Evaluation/Division of Anesthesiology, General Hospital, Respiratory, Infection Control and Dental Devices/Dental Devices Branch of the US Food and Drug Administration (FDA).

Mr. Steen is the team leader for implantable dental devices within the Dental Devices Branch and represents the FDA to both the American Dental Association Standard Committee for Dental Products and the International Organization for Standardization TC106 – Dentistry. 

Mr. Steen received a Bachelor of Science degree for Mechanical Engineering in 2002 from Rose-Hulman Institute of Technology in Terre Haute, Indiana, and conducted additional graduate work in Biomedical Engineering at Marquette University.  He interned as a manufacturing engineer at GE Appliances and worked as a dental laboratory technician at Lord’s Dental Studio in Wisconsin prior to joining the Dental Devices Branch as a scientific reviewer in 2005.  During his nine year tenure at the FDA, Mr. Steen has also worked in the Division of Toxicology in the Office of Science and Engineering Laboratory and the Division of Bioresearch Monitoring in the Office of Compliance.     

He has been recognized with the CDRH Scientific Achievement Award for Outstanding Intercenter Scientific Collaboration presented to FDA Intercenter Renal Biomarkers Group in 2006 & 2007 for the development of an intercenter systems biology approach for the investigation of sensitive and clinically relevant biomarkers for the early detection of kidney injury. He also received the FDA Outstanding Service Award in 2010 for developing, leading, and maintaining the endosseous implants rounds and working group within the Dental Devices Branch, and was granted FDA/CBER Group Recognition in 2011 with the Planning Committee for 1st FDA Regenerative Medicine Forum for extraordinary performance in organizing an outstanding FDA forum focused on Agency crosscutting issues in regulating regenerative medicine products.

   Speaker Events

Corporate Forum

Thursday, May 31

2:45 -3:45 pm


Plenary: Sterilization and Disinfection Updates

Friday, June 1                        DOWNLOAD PRESENTATION MATERIALS HERE

10:30 - 11:30 am


Plenary: Late-Breaker on National Guidance

Friday, June 1

4:30 - 5:30 pm


Early-Bird Workshop on OSAP Position Paper Dental Unit Waterlines

Saturday, June 2

6:30 - 7:30 am


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