Retrieve™ S292

GUDID 10810000526854

Mixing Tip with Brown Base for E.T.C.™ & Retrieve™ (Pkg. of 30 pcs.)

PARKELL, INC.

Dental material mixing nozzle, non-sterile Dental material mixing nozzle, non-sterile Dental material mixing nozzle, non-sterile Dental material mixing nozzle, non-sterile Dental material mixing nozzle, non-sterile Dental material mixing nozzle Dental material mixing nozzle Dental material mixing nozzle Dental material mixing nozzle Dental material mixing nozzle Dental material mixing nozzle Dental material mixing nozzle Dental material mixing nozzle Dental material mixing nozzle Dental material mixing nozzle Dental material mixing nozzle Dental material mixing nozzle Dental material mixing nozzle Dental material mixing nozzle Dental material mixing nozzle Dental material mixing nozzle Dental material mixing nozzle Dental material mixing nozzle Dental material mixing nozzle Dental material mixing nozzle Dental material mixing nozzle Dental material mixing nozzle Dental material mixing nozzle Dental material mixing nozzle Dental material mixing nozzle Dental material mixing nozzle Dental material mixing nozzle Dental material mixing nozzle Dental material mixing nozzle Dental material mixing nozzle Dental material mixing nozzle Dental material mixing nozzle Dental material mixing nozzle
Primary Device ID10810000526854
NIH Device Record Keyf99dbb02-53ce-491c-9469-02cea936017b
Commercial Distribution StatusIn Commercial Distribution
Brand NameRetrieve™
Version Model NumberS292
Catalog NumberS292
Company DUNS009900424
Company NamePARKELL, INC.
Device Count30
DM Exemptfalse
Pre-market Exemptfalse
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 Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone6312491134
Emailcustomerservice@parkell.com
Phone6312491134
Emailcustomerservice@parkell.com
Phone6312491134
Emailcustomerservice@parkell.com
Phone6312491134
Emailcustomerservice@parkell.com
Phone6312491134
Emailcustomerservice@parkell.com
Phone6312491134
Emailcustomerservice@parkell.com
Phone6312491134
Emailcustomerservice@parkell.com
Phone6312491134
Emailcustomerservice@parkell.com
Phone6312491134
Emailcustomerservice@parkell.com
Phone6312491134
Emailcustomerservice@parkell.com
Phone6312491134
Emailcustomerservice@parkell.com
Phone6312491134
Emailcustomerservice@parkell.com
Phone6312491134
Emailcustomerservice@parkell.com
Phone6312491134
Emailcustomerservice@parkell.com
Phone6312491134
Emailcustomerservice@parkell.com
Phone6312491134
Emailcustomerservice@parkell.com
Phone6312491134
Emailcustomerservice@parkell.com
Phone6312491134
Emailcustomerservice@parkell.com
Phone6312491134
Emailcustomerservice@parkell.com
Phone6312491134
Emailcustomerservice@parkell.com
Phone6312491134
Emailcustomerservice@parkell.com
Phone6312491134
Emailcustomerservice@parkell.com
Phone6312491134
Emailcustomerservice@parkell.com
Phone6312491134
Emailcustomerservice@parkell.com
Phone6312491134
Emailcustomerservice@parkell.com
Phone6312491134
Emailcustomerservice@parkell.com
Phone6312491134
Emailcustomerservice@parkell.com
Phone6312491134
Emailcustomerservice@parkell.com
Phone6312491134
Emailcustomerservice@parkell.com
Phone6312491134
Emailcustomerservice@parkell.com
Phone6312491134
Emailcustomerservice@parkell.com
Phone6312491134
Emailcustomerservice@parkell.com
Phone6312491134
Emailcustomerservice@parkell.com
Phone6312491134
Emailcustomerservice@parkell.com
Phone6312491134
Emailcustomerservice@parkell.com
Phone6312491134
Emailcustomerservice@parkell.com
Phone6312491134
Emailcustomerservice@parkell.com
Phone6312491134
Emailcustomerservice@parkell.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100810000526857 [Unit of Use]
GS110810000526854 [Primary]

FDA Product Code

EMACement, Dental

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2022-06-03
Device Publish Date2018-09-21

On-Brand Devices [Retrieve™]

M595S2500Retrieve™ Non-Eugenol Resin-Based Implant Cement
00810000525324Retrieve™ DC Non-Eugenol Resin-Based Implant Cement
00810000525621Retrieve™ DC Non-Eugenol Resin-Based Implant Cement (Korea)
10810000526854Mixing Tip with Brown Base for E.T.C.™ & Retrieve™ (Pkg. of 30 pcs.)

Trademark Results [Retrieve]

Mark Image

Registration | Serial
Company
Trademark
Application Date
RETRIEVE
RETRIEVE
90280683 not registered Live/Pending
Mumford Industries, Inc.
2020-10-27
RETRIEVE
RETRIEVE
87074209 5210881 Live/Registered
RETRIEVE TECHNOLOGIES, INC.
2016-06-16
RETRIEVE
RETRIEVE
86971430 5082049 Live/Registered
RETRIEVE TECHNOLOGIES, INC.
2016-04-11
RETRIEVE
RETRIEVE
86854000 5008032 Live/Registered
Midwest Distributing Summit Gold, Inc.
2015-12-18
RETRIEVE
RETRIEVE
85223504 4012246 Dead/Cancelled
Ingridients, Inc.
2011-01-21
RETRIEVE
RETRIEVE
78925945 3464453 Dead/Cancelled
TANDUS CENTIVA INC.
2006-07-10
RETRIEVE
RETRIEVE
78796927 not registered Dead/Abandoned
WILDERNESS ATHLETE, INC.
2006-01-23
RETRIEVE
RETRIEVE
78483838 not registered Dead/Abandoned
Dermatech Laboratories Pty Ltd
2004-09-15
RETRIEVE
RETRIEVE
78423914 not registered Dead/Abandoned
Agan Chemical Manufacturers Ltd.
2004-05-24
RETRIEVE
RETRIEVE
77747755 3822980 Live/Registered
Globus Medical, Inc.
2009-05-29
RETRIEVE
RETRIEVE
75529496 not registered Dead/Abandoned
Gonher De Mexico
1998-08-03
RETRIEVE
RETRIEVE
75502546 not registered Dead/Abandoned
Global Health, Inc.
1998-06-15

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