ReActive® Implant 754713

GUDID 10841307103714

Ø3.7 x 8 Platform 3.5mmD

IMPLANT DIRECT SYBRON MANUFACTURING LLC

Dental implant system
Primary Device ID10841307103714
NIH Device Record Keydb8e754d-b234-46de-9e0b-d80dfe9ec59f
Commercial Distribution StatusIn Commercial Distribution
Brand NameReActive® Implant
Version Model Number754713
Catalog Number754713
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
GS110841307103714 [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 [ReActive® Implant]

10841307103752Ø3.7 x 8 Platform 3.5mmD
10841307103745Ø3.7 x 8 Platform 3.5mmD
10841307103738Ø3.7 x 8 Platform 3.5mmD
10841307103721Ø3.7 x 8 Platform 3.5mmD
10841307103714Ø3.7 x 8 Platform 3.5mmD
10841307103707Ø3.7 x 8 Platform 3.5mmD
10841307103691Ø3.7 x 8 Platform 3.5mmD
10841307103684Ø3.7 x 8 Platform 3.5mmD
10841307103677Ø3.7 x 8 Platform 3.5mmD
10841307103660Ø3.7 x 8 Platform 3.5mmD
10841307103653Ø3.7 x 8 Platform 3.5mmD
10841307103646Ø3.7 x 8 Platform 3.5mmD
10841307103639Ø3.7 x 8 Platform 3.5mmD
10841307103622Ø3.7 x 8 Platform 3.5mmD
10841307103615Ø3.7 x 8 Platform 3.5mmD
10841307103608Ø3.7 x 8 Platform 3.5mmD
10841307103592Ø3.7 x 8 Platform 3.5mmD
10841307103585Ø3.7 x 8 Platform 3.5mmD

Trademark Results [ReActive]

Mark Image

Registration | Serial
Company
Trademark
Application Date
REACTIVE
REACTIVE
98312957 not registered Live/Pending
Anvil Rods LLC
2023-12-13
REACTIVE
REACTIVE
90349352 not registered Live/Pending
Threads for Thought, LLC
2020-11-30
REACTIVE
REACTIVE
88759769 not registered Live/Pending
Vera Bradley Designs, Inc.
2020-01-15
REACTIVE
REACTIVE
88757347 not registered Live/Pending
IMPLANT DIRECT SYBRON INTERNATIONAL LLC
2020-01-13
REACTIVE
REACTIVE
86876980 not registered Dead/Abandoned
Su, Xiao
2016-01-15
REACTIVE
REACTIVE
79103539 4244000 Dead/Cancelled
Accenture Global Services Ltd
2011-05-06
REACTIVE
REACTIVE
79033854 3307628 Dead/Cancelled
REACTIVE SPORTS COMPANY PTE LTD
2006-07-07
REACTIVE
REACTIVE
79015012 not registered Dead/Abandoned
REAKTIF TEKSTIL SANAYI VE TICARET LIMITED SIRKETI
2005-05-17
REACTIVE
REACTIVE
79003341 not registered Dead/Cancelled
REAKTIF TEKSTIL SANAYI VE TICARET LIMITED SIRKETI
2004-06-18
REACTIVE
REACTIVE
77404387 3652116 Live/Registered
IMPLANT DIRECT SYBRON INTERNATIONAL LLC
2008-02-22
REACTIVE
REACTIVE
77012281 3496381 Dead/Cancelled
GEODynamics, Inc.
2006-10-03
REACTIVE
REACTIVE
75463604 2349328 Dead/Cancelled
HANSBERGER PRECISION GOLF, INC.
1998-04-07

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