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Dio Corporation

FDA 510(k) & PMA Approved Devices — 14 products

Total Devices14
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K220253 Eco Abutment, Multiunit AbutmentNHA2023-08-18 View
510(k) K210828 DIOnavi-Denture02EBI2021-03-23 View
510(k) K193623 DIOnavi-DentureEBI2020-10-22 View
510(k) K193404 UF(II) Bar holder abutmentNHA2020-05-18 View
510(k) K192263 UCLA CCM AbutmentNHA2020-02-21 View
510(k) K190048 UF(II) Anatomic abutmentNHA2019-09-30 View
510(k) K181037 DIO CAD/CAM AbutmentNHA2018-12-21 View
510(k) K182194 UV Active Implant SystemDZE2018-12-14 View
510(k) K173975 UF(II) Wide FixtureDZE2018-06-01 View
510(k) K170608 UF(II) Implant SystemDZE2018-03-30 View
510(k) K161987 UF(II) Narrow Implant System - Fixture, UF(II) Narrow Implant System - SuprastructureDZE2017-02-21 View
510(k) K122519 DIO UF HSA INTERNAL SUB-MERGED IMPLANT SYSTEMDZE2013-05-21 View
510(k) K112746 DIOSLIMON IMPLANT SYSTEMDZE2011-10-21 View
510(k) K100100 DIO STEADY EXTERNAL IMPLANT SYSTEMDZE2010-11-10 View
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