DIOnavi Guide

GUDID 08800049414279

DIO Corporation

Dental guided surgery reference plate
Primary Device ID08800049414279
NIH Device Record Key441fea1d-23e2-43c0-88d6-672e15400544
Commercial Distribution StatusIn Commercial Distribution
Brand NameDIOnavi Guide
Version Model NumberGUIDE 02 A04(a,b)
Company DUNS631085206
Company NameDIO Corporation
Device Count1
DM Exempttrue
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS108800049414279 [Primary]

FDA Product Code

NDPAccessories, Implant, Dental, Endosseous

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[08800049414279]

Moist Heat or Steam Sterilization


[08800049414279]

Moist Heat or Steam Sterilization


[08800049414279]

Moist Heat or Steam Sterilization


[08800049414279]

Moist Heat or Steam Sterilization


[08800049414279]

Moist Heat or Steam Sterilization


[08800049414279]

Moist Heat or Steam Sterilization


[08800049414279]

Moist Heat or Steam Sterilization


[08800049414279]

Moist Heat or Steam Sterilization


[08800049414279]

Moist Heat or Steam Sterilization


[08800049414279]

Moist Heat or Steam Sterilization


[08800049414279]

Moist Heat or Steam Sterilization


[08800049414279]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2025-09-26
Device Publish Date2025-09-18

On-Brand Devices [DIOnavi Guide]

08800049414293GUIDE 02 A05(a,b)
08800049414279GUIDE 02 A04(a,b)
08800049414255GUIDE 02 A03(a,b)
08800049414231GUIDE 02 A02(a,b)
08800049414217GUIDE 02 A01(a,b)

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