FDA 510(k) Applications Submitted by OSSTELL AB

FDA 510(k) Number Submission Date Device Name Applicant
K132401 08/01/2013 MEGA ISQ OSSTELL AB
K082523 09/02/2008 OSSTELL ISQ IMPLANT STABILITY METER OSSTELL AB
K142358 08/25/2014 Osstell IDx OSSTELL AB
K181888 07/13/2018 Osstell Beacon Osstell AB


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