FDA 510(k) Applications Submitted by HiOSSEN Inc.

FDA 510(k) Number Submission Date Device Name Applicant
K170421 02/13/2017 ET Hybrid Abutment Hiossen Inc.
K151542 06/08/2015 A-Oss HIOSSEN INC.
K151626 06/17/2015 ET III Bio-SA Fixture System HiOSSEN Inc.
K162390 08/26/2016 ET Hybrid Abutment HIOSSEN INC.
K090237 02/02/2009 HG II FIXTURE SYSTEM HIOSSEN INC.
K140934 04/11/2014 HIOSSEN IMPLANT SYSTEM HIOSSEN INC.
K101096 04/20/2010 HT III SA FIXTURE SYSTEM HIOSSEN INC.
K132067 07/03/2013 MULTI ANGLED ABUTMENT SYSTEM HIOSSEN INC.
K112532 08/31/2011 ET II BIO-SA FIXTURE SYSTEM HIOSSEN INC.
K093352 10/27/2009 HG III FIXTURE SYSTEM HIOSSEN INC.
K123471 11/13/2012 ETII SA FIXTURE SYSTEM HIOSSEN INC.
K153332 11/19/2015 ETIII SA Fixture System (O3.2mm) HIOSSEN INC.
K123627 11/23/2012 ET SMARTFIT ABUTMENT HIOSSEN INC.
K103537 12/02/2010 ET III SA ULTRA WIDE SYSTEM HIOSSEN INC.
K093889 12/18/2009 MODIFICATION TO: HG III ULTRA WIDE SYSTEM HIOSSEN INC.
K222636 08/31/2022 ET Abutment System Hiossen Inc.


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