Atlas FDA

Dio Corporation

14 FDA 510(k) clearances · Manufacturer

Sort:Newest firstOldest first

Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free

RecordFirmDate
Eco Abutment, Multiunit Abutment (K220253)Dio Corporation2023-08-18
DIOnavi-Denture02 (K210828)Dio Corporation2021-03-23
DIOnavi-Denture (K193623)Dio Corporation2020-10-22
UF(II) Bar holder abutment (K193404)Dio Corporation2020-05-18
UCLA CCM Abutment (K192263)Dio Corporation2020-02-21
UF(II) Anatomic abutment (K190048)Dio Corporation2019-09-30
DIO CAD/CAM Abutment (K181037)Dio Corporation2018-12-21
UV Active Implant System (K182194)Dio Corporation2018-12-14
UF(II) Wide Fixture (K173975)Dio Corporation2018-06-01
UF(II) Implant System (K170608)Dio Corporation2018-03-30
UF(II) Narrow Implant System - Fixture, UF(II) Narrow Implant System - Suprastructure (K161987)Dio Corporation2017-02-21
DIO UF HSA INTERNAL SUB-MERGED IMPLANT SYSTEM (K122519)Dio Corporation2013-05-21
DIOSLIMON IMPLANT SYSTEM (K112746)Dio Corporation2011-10-21
DIO STEADY EXTERNAL IMPLANT SYSTEM (K100100)Dio Corporation2010-11-10

Track Dio Corporation automatically

Every clearance here is in the API, with alerts when new ones post.