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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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