Dio Corporation
14 FDA 510(k) clearances · Manufacturer
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| Record | Firm | Date |
|---|---|---|
| Eco Abutment, Multiunit Abutment (K220253) | Dio Corporation | 2023-08-18 |
| DIOnavi-Denture02 (K210828) | Dio Corporation | 2021-03-23 |
| DIOnavi-Denture (K193623) | Dio Corporation | 2020-10-22 |
| UF(II) Bar holder abutment (K193404) | Dio Corporation | 2020-05-18 |
| UCLA CCM Abutment (K192263) | Dio Corporation | 2020-02-21 |
| UF(II) Anatomic abutment (K190048) | Dio Corporation | 2019-09-30 |
| DIO CAD/CAM Abutment (K181037) | Dio Corporation | 2018-12-21 |
| UV Active Implant System (K182194) | Dio Corporation | 2018-12-14 |
| UF(II) Wide Fixture (K173975) | Dio Corporation | 2018-06-01 |
| UF(II) Implant System (K170608) | Dio Corporation | 2018-03-30 |
| UF(II) Narrow Implant System - Fixture, UF(II) Narrow Implant System - Suprastructure (K161987) | Dio Corporation | 2017-02-21 |
| DIO UF HSA INTERNAL SUB-MERGED IMPLANT SYSTEM (K122519) | Dio Corporation | 2013-05-21 |
| DIOSLIMON IMPLANT SYSTEM (K112746) | Dio Corporation | 2011-10-21 |
| DIO STEADY EXTERNAL IMPLANT SYSTEM (K100100) | Dio Corporation | 2010-11-10 |
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Every clearance here is in the API, with alerts when new ones post.