FDA 510(k) Applications Submitted by Viviana Horhoiu

FDA 510(k) Number	Submission Date	Device Name	Applicant
K190082	01/17/2019	Straumann BLX Variobase Abutment	Institut Straumann AG
K220751	03/15/2022	Straumann BLX Temporary Abutment, VITA CAD-Temp, PMMA	Institut Straumann AG
K210855	03/23/2021	Straumann BLX Implant System	Institut Straumann AG
K211052	04/09/2021	Straumann RidgeFit Implants	Institut Straumann AG
K201681	06/22/2020	Straumann Immediate Temporary Abutments	Institut Straumann AG
K181703	06/27/2018	Straumann BLX Line Extension - Implants, SRAs and Anatomic Abutments	Institut Straumann AG
K191895	07/15/2019	Straumann Mini Implants	Institut Straumann AG
K173961	12/28/2017	Straumann BLX Implant System	Institut Straumann AG