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Dio Corporation

FDA 510(k) & PMA Approved Devices — 11 products

Total Devices11
Categories3
Latest Approval2023-08-18
TypeNumberDevice NameCodeDate
510(k) K220253 Eco Abutment, Multiunit Abutment NHA 2023-08-18 View
510(k) K210828 DIOnavi-Denture02 EBI 2021-03-23 View
510(k) K193623 DIOnavi-Denture EBI 2020-10-22 View
510(k) K193404 UF(II) Bar holder abutment NHA 2020-05-18 View
510(k) K192263 UCLA CCM Abutment NHA 2020-02-21 View
510(k) K190048 UF(II) Anatomic abutment NHA 2019-09-30 View
510(k) K181037 DIO CAD/CAM Abutment NHA 2018-12-21 View
510(k) K182194 UV Active Implant System DZE 2018-12-14 View
510(k) K173975 UF(II) Wide Fixture DZE 2018-06-01 View
510(k) K170608 UF(II) Implant System DZE 2018-03-30 View
510(k) K161987 UF(II) Narrow Implant System - Fixture, UF(II) Narrow Implant System - Suprastructure DZE 2017-02-21 View
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