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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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