Dio Corporation
FDA 510(k) medical device clearances.
Top product codes for Dio Corporation
Recent clearances by Dio Corporation
- K220253 — Eco Abutment, Multiunit Abutment
- K210828 — DIOnavi-Denture02
- K193623 — DIOnavi-Denture
- K193404 — UF(II) Bar holder abutment
- K192263 — UCLA CCM Abutment
- K190048 — UF(II) Anatomic abutment
- K181037 — DIO CAD/CAM Abutment
- K182194 — UV Active Implant System
- K173975 — UF(II) Wide Fixture
- K170608 — UF(II) Implant System
- K161987 — UF(II) Narrow Implant System - Fixture, UF(II) Narrow Implant System - Suprastructure
- K122519 — DIO UF HSA INTERNAL SUB-MERGED IMPLANT SYSTEM
- K112746 — DIOSLIMON IMPLANT SYSTEM
- K100100 — DIO STEADY EXTERNAL IMPLANT SYSTEM
Data sourced from openFDA. This site is unofficial and independent of the FDA.