Dio Corporation
Dio Corporation appears in FDA public data with 0 recalls, 14 510(k) clearances, 1 FDA inspection, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on August 18, 2023.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 14
- Inspections
- 1
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K220253 | Eco Abutment, Multiunit Abutment | August 18, 2023 |
| K210828 | DIOnavi-Denture02 | March 23, 2021 |
| K193623 | DIOnavi-Denture | October 22, 2020 |
| K193404 | UF(II) Bar holder abutment | May 18, 2020 |
| K192263 | UCLA CCM Abutment | February 21, 2020 |
| K190048 | UF(II) Anatomic abutment | September 30, 2019 |
| K181037 | DIO CAD/CAM Abutment | December 21, 2018 |
| K182194 | UV Active Implant System | December 14, 2018 |
| K173975 | UF(II) Wide Fixture | June 1, 2018 |
| K170608 | UF(II) Implant System | March 30, 2018 |
| K161987 | UF(II) Narrow Implant System - Fixture, UF(II) Narrow Implant System - Suprastructure | February 21, 2017 |
| K122519 | DIO UF HSA INTERNAL SUB-MERGED IMPLANT SYSTEM | May 21, 2013 |
| K112746 | DIOSLIMON IMPLANT SYSTEM | October 21, 2011 |
| K100100 | DIO STEADY EXTERNAL IMPLANT SYSTEM | November 10, 2010 |