FDA 510(k) Applications Submitted by KIEN T. NGUYEN

FDA 510(k) Number Submission Date Device Name Applicant
K162306 08/17/2016 SomnoDent ALPHA SomnoMed Inc.
K150369 02/13/2015 SomnoDent Classic with DentiTrac Micro-recorder, SomnoDent Flex with DentiTrac Micro-recorder, SomnoDent Herbst Advance (Classic or Flex Retention) with DentiTrac Micro-recorder, SomnoDent G2 (Classic or Flex Retention) with DentiTrac Micro-recorder, Somn SOMNOMED INC.


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