FDA 510(k) Applications Submitted by DIO CORPORATION

FDA 510(k) Number	Submission Date	Device Name	Applicant
K220253	01/31/2022	Eco Abutment, Multiunit Abutment	DIO Corporation
K210828	03/19/2021	DIOnavi-Denture02	DIO Corporation
K190048	01/10/2019	UF(II) Anatomic abutment	DIO Corporation
K170608	03/01/2017	UF(II) Implant System	DIO Corporation
K181037	04/19/2018	DIO CAD/CAM Abutment	DIO Corporation
K192263	08/21/2019	UCLA CCM Abutment	DIO Corporation
K193404	12/06/2019	UF(II) Bar holder abutment	DIO Corporation
K193623	12/26/2019	DIOnavi-Denture	DIO Corporation
K173975	12/29/2017	UF(II) Wide Fixture	DIO Corporation
K182194	08/14/2018	UV Active Implant System	DIO Corporation
K161987	07/19/2016	UF(II) Narrow Implant System - Fixture, UF(II) Narrow Implant System - Suprastructure	DIO CORPORATION
K100100	01/12/2010	DIO STEADY EXTERNAL IMPLANT SYSTEM	DIO CORPORATION
K122519	08/17/2012	DIO UF HSA INTERNAL SUB-MERGED IMPLANT SYSTEM	DIO CORPORATION
K112746	09/21/2011	DIOSLIMON IMPLANT SYSTEM	DIO CORPORATION