simplyCrown&Bridge Legacy™ Narrow 8745-23N

GUDID 10841307112631

IMPLANT DIRECT SYBRON MANUFACTURING LLC

Dental implant suprastructure, permanent, preformed
Primary Device ID10841307112631
NIH Device Record Key38e2db83-5036-4d2d-ba6c-3ac5b0d9f70a
Commercial Distribution StatusIn Commercial Distribution
Brand NamesimplyCrown&Bridge Legacy™ Narrow
Version Model Number8745-23N
Catalog Number8745-23N
Company DUNS868856969
Company NameIMPLANT DIRECT SYBRON MANUFACTURING LLC
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kittrue
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone1-888-649-6425
Emailcustomerservice@implantdirect.com

Device Dimensions

Device Size Text, specify0

Device Identifiers

Device Issuing AgencyDevice ID
GS110841307112631 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

NHAAbutment, Implant, Dental, Endosseous

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[10841307112631]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number5
Public Version Date2019-11-08
Device Publish Date2015-09-14

On-Brand Devices [simplyCrown&Bridge Legacy™ Narrow]

108413071126628757-23N
108413071126558757-22N
108413071126488757-21N
108413071126318745-23N
108413071126248745-22N
108413071126178745-21N
108413071126008735-23N
108413071125948735-22N
108413071125878735-21N

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