Scan Post 260-100-830

GUDID 00813110029768

3.0mm Titanium Scan Post (2)

BICON, LLC

Dental implant abutment analog, scanning
Primary Device ID00813110029768
NIH Device Record Key29c22d56-91d9-4323-b3b8-9a8747f3e01e
Commercial Distribution StatusIn Commercial Distribution
Brand NameScan Post
Version Model Number260-100-830
Catalog Number260-100-830
Company DUNS945015758
Company NameBICON, LLC
Device Count1
DM Exemptfalse
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 Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone617-524-4443
Emailsupport@bicon.com
Phone617-524-4443
Emailsupport@bicon.com
Phone617-524-4443
Emailsupport@bicon.com
Phone617-524-4443
Emailsupport@bicon.com
Phone617-524-4443
Emailsupport@bicon.com
Phone617-524-4443
Emailsupport@bicon.com
Phone617-524-4443
Emailsupport@bicon.com
Phone617-524-4443
Emailsupport@bicon.com
Phone617-524-4443
Emailsupport@bicon.com
Phone617-524-4443
Emailsupport@bicon.com
Phone617-524-4443
Emailsupport@bicon.com
Phone617-524-4443
Emailsupport@bicon.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100813110029768 [Primary]

FDA Product Code

NDPAccessories, Implant, Dental, Endosseous

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2024-10-29
Device Publish Date2024-10-21

On-Brand Devices [Scan Post]

008131100273203.0mm Scan Post (2)
008131100273132.5mm Scan Post (2)
008131100273062.0mm Scan Post (2)
008131100297683.0mm Titanium Scan Post (2)
008131100297512.5mm Titanium Scan Post (2)
008131100297442.0mm Titanium Scan Post (2)

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