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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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