FibreKor

GUDID 10814978021021

Fiber Post; 1.375 mm Posts

Kerr Corporation

Root canal post, preformed Root canal post, preformed Root canal post, preformed Root canal post, preformed Root canal post, preformed Root canal post, preformed Root canal post, preformed Root canal post, preformed Root canal post, preformed Root canal post, preformed Root canal post, preformed Root canal post, preformed Root canal post, preformed Root canal post, preformed Root canal post, preformed Root canal post, preformed
Primary Device ID10814978021021
NIH Device Record Keydb7e5333-fca0-4a34-bc04-df516c706bd0
Commercial Distribution StatusIn Commercial Distribution
Brand NameFibreKor
Version Model NumberN18AE
Company DUNS199354556
Company NameKerr Corporation
Device Count30
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 Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+18005377123
Emailcustomercare@kavokerrgroup.com
Phone+18005377123
Emailcustomercare@kavokerrgroup.com
Phone+18005377123
Emailcustomercare@kavokerrgroup.com
Phone+18005377123
Emailcustomercare@kavokerrgroup.com
Phone+18005377123
Emailcustomercare@kavokerrgroup.com
Phone+18005377123
Emailcustomercare@kavokerrgroup.com
Phone+18005377123
Emailcustomercare@kavokerrgroup.com
Phone+18005377123
Emailcustomercare@kavokerrgroup.com
Phone+18005377123
Emailcustomercare@kavokerrgroup.com
Phone+18005377123
Emailcustomercare@kavokerrgroup.com
Phone+18005377123
Emailcustomercare@kavokerrgroup.com
Phone+18005377123
Emailcustomercare@kavokerrgroup.com
Phone+18005377123
Emailcustomercare@kavokerrgroup.com
Phone+18005377123
Emailcustomercare@kavokerrgroup.com
Phone+18005377123
Emailcustomercare@kavokerrgroup.com
Phone+18005377123
Emailcustomercare@kavokerrgroup.com

Device Dimensions

Outer Diameter1.375 Millimeter
Outer Diameter1.375 Millimeter
Outer Diameter1.375 Millimeter
Outer Diameter1.375 Millimeter
Outer Diameter1.375 Millimeter
Outer Diameter1.375 Millimeter
Outer Diameter1.375 Millimeter
Outer Diameter1.375 Millimeter
Outer Diameter1.375 Millimeter
Outer Diameter1.375 Millimeter
Outer Diameter1.375 Millimeter
Outer Diameter1.375 Millimeter
Outer Diameter1.375 Millimeter
Outer Diameter1.375 Millimeter
Outer Diameter1.375 Millimeter
Outer Diameter1.375 Millimeter

Operating and Storage Conditions

Storage Environment TemperatureBetween 2 Degrees Celsius and 25 Degrees Celsius
Storage Environment TemperatureBetween 2 Degrees Celsius and 25 Degrees Celsius
Storage Environment TemperatureBetween 2 Degrees Celsius and 25 Degrees Celsius
Storage Environment TemperatureBetween 2 Degrees Celsius and 25 Degrees Celsius
Storage Environment TemperatureBetween 2 Degrees Celsius and 25 Degrees Celsius
Storage Environment TemperatureBetween 2 Degrees Celsius and 25 Degrees Celsius
Storage Environment TemperatureBetween 2 Degrees Celsius and 25 Degrees Celsius
Storage Environment TemperatureBetween 2 Degrees Celsius and 25 Degrees Celsius
Storage Environment TemperatureBetween 2 Degrees Celsius and 25 Degrees Celsius
Storage Environment TemperatureBetween 2 Degrees Celsius and 25 Degrees Celsius
Storage Environment TemperatureBetween 2 Degrees Celsius and 25 Degrees Celsius
Storage Environment TemperatureBetween 2 Degrees Celsius and 25 Degrees Celsius
Storage Environment TemperatureBetween 2 Degrees Celsius and 25 Degrees Celsius
Storage Environment TemperatureBetween 2 Degrees Celsius and 25 Degrees Celsius
Storage Environment TemperatureBetween 2 Degrees Celsius and 25 Degrees Celsius
Storage Environment TemperatureBetween 2 Degrees Celsius and 25 Degrees Celsius

Device Identifiers

Device Issuing AgencyDevice ID
GS100814978021024 [Unit of Use]
GS110814978021021 [Primary]

FDA Product Code

ELRPOST, ROOT CANAL

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2021-12-09
Device Publish Date2016-08-01

On-Brand Devices [FibreKor]

00814978023219Fiber Post; 10x 1.00 mm, 1.25 mm, 1.50 mm Posts
00814978020973Tapered Post; 1.50 mm Drill
00814978020966Tapered Post; 1.375 mm Drill
00814978020959Post; 1.25 mm Drill
00814978020935Fiber Post; 1.375 mm Drill
00814978020911Fiber Post; 1.125 mm Drill
00814978020898Fiber Post; 1.50 mm Drill
00814978020874Fiber Post; 1.25 mm Drill
00814978020850Fiber Post; 1.00 mm Drill
10814978023209Fiber Post; Kit; 5x 1.00 mm, 1.25 mm, 1.50 mm Posts; 1x 1.00 mm, 1.25 mm, 1.50 mm Drills
10814978021083Fiber Post; 1.375 mm Posts
10814978021076Fiber Post; 1.125 mm Posts
10814978021069Fiber Post; 1.50 mm Posts
10814978021052Fiber Post; 1.25 mm Posts
10814978021045Fiber Post; 1.00 mm Posts
10814978021038Fiber Post; 1.50 mm Posts
10814978021021Fiber Post; 1.375 mm Posts
10814978021014Fiber Post; 1.25 mm Posts
10814978021007Fiber Post; 1.125 mm Posts
10814978020994Fiber Post; 1.00 mm Posts

Trademark Results [FibreKor]

Mark Image

Registration | Serial
Company
Trademark
Application Date
FIBREKOR
FIBREKOR
86325180 not registered Dead/Abandoned
Pentron Corporation
2014-07-01
FIBREKOR
FIBREKOR
78884620 3302191 Dead/Cancelled
Jeneric/Pentron
2006-05-16
FIBREKOR
FIBREKOR
75181389 2127868 Live/Registered
Jeneric/Pentron Incorporated
1996-10-15

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