Scan Post 260-100-810

GUDID 00813110029744

2.0mm Titanium Scan Post (2)

BICON, LLC

Dental implant abutment analog, scanning
Primary Device ID00813110029744
NIH Device Record Key63250e8d-6dcc-41ba-a52d-0c8c58c7a777
Commercial Distribution StatusIn Commercial Distribution
Brand NameScan Post
Version Model Number260-100-810
Catalog Number260-100-810
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
GS100813110029744 [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)

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.