Multi Angled Abutment MAA 483520H

GUDID 08800049251003

DIO Corporation

Dental implant suprastructure, permanent, preformed
Primary Device ID08800049251003
NIH Device Record Key73856441-9f90-4fac-856e-2c98601dbd25
Commercial Distribution StatusIn Commercial Distribution
Brand NameMulti Angled Abutment
Version Model NumberMAA 483520H
Catalog NumberMAA 483520H
Company DUNS631085206
Company NameDIO Corporation
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numbertrue
Manufacturing Datetrue
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS108800049251003 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

NHAAbutment, Implant, Dental, Endosseous

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[08800049251003]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-03-18
Device Publish Date2020-03-10

On-Brand Devices [Multi Angled Abutment]

08800049251102MAA 485530H
08800049251089MAA 485520H
08800049251065MAA 484530H
08800049251041MAA 484520H
08800049251027MAA 483530H
08800049251003MAA 483520H
08800049250983MAA 482520H

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