LINX PROCEDURE

The LINX Device was first approved by the FDA for use in 2007 based upon published series of safety and outcome data.  Dr. Chiasson began offering this procedure in 2015 after additional long-term published data reinforced the earlier results.  Since then, he has embraced the use of this device for those individuals seeking a solution to their issues with GERD/LPRD and has developed an extensive experience with this procedure over the years.