Custom RePlant Titanium Abutment 6035-31-XX

GUDID 10841307116783

IMPLANT DIRECT SYBRON MANUFACTURING LLC

Dental implant suprastructure, permanent, preformed
Primary Device ID10841307116783
NIH Device Record Key317e26db-b6b2-4ee8-a742-2a95a4c7317b
Commercial Distribution Discontinuation2018-12-31
Commercial Distribution StatusNot in Commercial Distribution
Brand NameCustom RePlant Titanium Abutment
Version Model Number6035-31-XX
Catalog Number6035-31-XX
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
GS110841307116783 [Primary]

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[10841307116783]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number6
Public Version Date2019-11-08
Device Publish Date2015-09-23

On-Brand Devices [Custom RePlant Titanium Abutment]

108413071168066050-31-XX
108413071167906043-31-XX
108413071167836035-31-XX
108413071168136060-31-XX

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