Vulcan Custom Dental

GUDID 00810033850530

Elos Accurate® Custom Ti Abut, Nobel Branemark NP

VULCAN CUSTOM DENTAL, INC

Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed
Primary Device ID00810033850530
NIH Device Record Key4b12c75f-0334-436f-8be2-7ab8997a9279
Commercial Distribution StatusIn Commercial Distribution
Brand NameVulcan Custom Dental
Version Model NumberTIABUT317
Company DUNS080285276
Company NameVULCAN CUSTOM DENTAL, INC
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 Numberfalse
Manufacturing Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latextrue
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100810033850530 [Primary]
GS100810033850530 [Primary]
GS100810033850530 [Primary]
GS100810033850530 [Primary]
GS100810033850530 [Primary]
GS100810033850530 [Primary]
GS100810033850530 [Primary]
GS100810033850530 [Primary]
GS100810033850530 [Primary]
GS100810033850530 [Primary]
GS100810033850530 [Primary]
GS100810033850530 [Primary]
GS100810033850530 [Primary]
GS100810033850530 [Primary]
GS100810033850530 [Primary]

FDA Product Code

NHAAbutment, Implant, Dental, Endosseous
NHAAbutment, Implant, Dental, Endosseous
NHAAbutment, Implant, Dental, Endosseous
NHAAbutment, Implant, Dental, Endosseous
NHAAbutment, Implant, Dental, Endosseous
NHAAbutment, Implant, Dental, Endosseous
NHAAbutment, Implant, Dental, Endosseous
NHAAbutment, Implant, Dental, Endosseous
NHAAbutment, Implant, Dental, Endosseous
NHAAbutment, Implant, Dental, Endosseous
NHAAbutment, Implant, Dental, Endosseous
NHAAbutment, Implant, Dental, Endosseous
NHAAbutment, Implant, Dental, Endosseous
NHAAbutment, Implant, Dental, Endosseous
NHAAbutment, Implant, Dental, Endosseous

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00810033850530]

Moist Heat or Steam Sterilization


[00810033850530]

Moist Heat or Steam Sterilization


[00810033850530]

Moist Heat or Steam Sterilization


[00810033850530]

Moist Heat or Steam Sterilization


[00810033850530]

Moist Heat or Steam Sterilization


[00810033850530]

Moist Heat or Steam Sterilization


[00810033850530]

Moist Heat or Steam Sterilization


[00810033850530]

Moist Heat or Steam Sterilization


[00810033850530]

Moist Heat or Steam Sterilization


[00810033850530]

Moist Heat or Steam Sterilization


[00810033850530]

Moist Heat or Steam Sterilization


[00810033850530]

Moist Heat or Steam Sterilization


[00810033850530]

Moist Heat or Steam Sterilization


[00810033850530]

Moist Heat or Steam Sterilization


[00810033850530]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-06-23
Device Publish Date2020-06-15

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