RePlant® Implant 603513

GUDID 10841307104018

Ø3.7 x 8 Platform 3.5mmD

IMPLANT DIRECT SYBRON MANUFACTURING LLC

Dental implant system
Primary Device ID10841307104018
NIH Device Record Key20ca3e81-c42a-4d41-aa1e-9f374996f3dd
Commercial Distribution StatusIn Commercial Distribution
Brand NameRePlant® Implant
Version Model Number603513
Catalog Number603513
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 Datetrue
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
Phone1-888-649-6425
Emailcustomerservice@implantdirect.com
Phone1-888-649-6425
Emailcustomerservice@implantdirect.com
Phone1-888-649-6425
Emailcustomerservice@implantdirect.com
Phone1-888-649-6425
Emailcustomerservice@implantdirect.com
Phone1-888-649-6425
Emailcustomerservice@implantdirect.com
Phone1-888-649-6425
Emailcustomerservice@implantdirect.com
Phone1-888-649-6425
Emailcustomerservice@implantdirect.com
Phone1-888-649-6425
Emailcustomerservice@implantdirect.com
Phone1-888-649-6425
Emailcustomerservice@implantdirect.com
Phone1-888-649-6425
Emailcustomerservice@implantdirect.com
Phone1-888-649-6425
Emailcustomerservice@implantdirect.com

Device Dimensions

Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0

Device Identifiers

Device Issuing AgencyDevice ID
GS110841307104018 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

DZEImplant, Endosseous, Root-Form

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2024-12-20
Device Publish Date2015-09-14

On-Brand Devices [RePlant® Implant]

10841307104162Ø3.7 x 8 Platform 3.5mmD
10841307104155Ø3.7 x 8 Platform 3.5mmD
10841307104148Ø3.7 x 8 Platform 3.5mmD
10841307104131Ø3.7 x 8 Platform 3.5mmD
10841307104124Ø3.7 x 8 Platform 3.5mmD
10841307104117Ø3.7 x 8 Platform 3.5mmD
10841307104100Ø3.7 x 8 Platform 3.5mmD
10841307104094Ø3.7 x 8 Platform 3.5mmD
10841307104087Ø3.7 x 8 Platform 3.5mmD
10841307104070Ø3.7 x 8 Platform 3.5mmD
10841307104063Ø3.7 x 8 Platform 3.5mmD
10841307104056Ø3.7 x 8 Platform 3.5mmD
10841307104049Ø3.7 x 8 Platform 3.5mmD
10841307104032Ø3.7 x 8 Platform 3.5mmD
10841307104025Ø3.7 x 8 Platform 3.5mmD
10841307104018Ø3.7 x 8 Platform 3.5mmD
10841307104001Ø3.7 x 8 Platform 3.5mmD
10841307103998Ø3.7 x 8 Platform 3.5mmD
10841307103981Ø3.7 x 8 Platform 3.5mmD

Trademark Results [RePlant]

Mark Image

Registration | Serial
Company
Trademark
Application Date
REPLANT
REPLANT
97914673 not registered Live/Pending
Von Holzhausen
2023-05-01
REPLANT
REPLANT
97914671 not registered Live/Pending
Von Holzhausen
2023-05-01
REPLANT
REPLANT
97036376 not registered Live/Pending
Strange Attractor, LLC
2021-09-20
REPLANT
REPLANT
88518101 not registered Live/Pending
Michelle MacRae
2019-07-17
REPLANT
REPLANT
77097406 not registered Dead/Abandoned
Implant Direct LLC
2007-02-01
REPLANT
REPLANT
76628186 3344697 Live/Registered
IMPLANT DIRECT SYBRON INTERNATIONAL LLC
2005-01-19
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.