Medical Device Manufacturer · US , Los Angeles , CA

Dio Corporation - FDA 510(k) Cleared Devices

14 submissions · 14 cleared · Since 2010

Total

Cleared

Denied

Dio Corporation has 14 FDA 510(k) cleared dental devices. Based in Los Angeles, US.

Last cleared in 2023. Active since 2010.

Browse the complete list of FDA 510(k) cleared dental devices from this manufacturer. Filter by specialty or product code using the sidebar.

FDA 510(k) cleared devices by Dio Corporation

14 devices

1-12 of 14

Cleared Aug 18, 2023

Eco Abutment, Multiunit Abutment

UF(II) Bar holder abutment

UF(II) Anatomic abutment

UV Active Implant System

UF(II) Implant System

K170608 · DZE

Dental · 394d

Cleared Feb 21, 2017

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

K161987 · DZE

Dental · 217d

Cleared May 21, 2013

DIO UF HSA INTERNAL SUB-MERGED IMPLANT SYSTEM

K122519 · DZE

Dental · 277d

Dio Corporation - FDA 510(k) Cleared Devices

FDA 510(k) cleared devices by Dio Corporation

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