Medical Device Manufacturer · US , Los Angeles , CA

Dio Corporation - FDA 510(k) Cleared Devices

14 submissions · 14 cleared · Since 2010

14

Total

14

Cleared

0

Denied

FDA 510(k) cleared devices by Dio Corporation Dental ✕

14 devices

1-14 of 14

Cleared Aug 18, 2023

Eco Abutment, Multiunit Abutment

Cleared Mar 23, 2021

DIOnavi-Denture02

Cleared Oct 22, 2020

DIOnavi-Denture

Cleared May 18, 2020

UF(II) Bar holder abutment

Cleared Feb 21, 2020

UCLA CCM Abutment

Cleared Sep 30, 2019

UF(II) Anatomic abutment

Cleared Dec 21, 2018

DIO CAD/CAM Abutment

Cleared Dec 14, 2018

UV Active Implant System

Cleared Jun 01, 2018

UF(II) Wide Fixture

Cleared Mar 30, 2018

UF(II) Implant System

Cleared Feb 21, 2017

UF(II) Narrow Implant System - Fixture, UF(II) Narrow Implant System -...

Cleared May 21, 2013

DIO UF HSA INTERNAL SUB-MERGED IMPLANT SYSTEM

Cleared Oct 21, 2011

DIOSLIMON IMPLANT SYSTEM

Cleared Nov 10, 2010

DIO STEADY EXTERNAL IMPLANT SYSTEM