Zimmer ZFX Component

GUDID 00889024020696

ZIMMER DENTAL INC.

Dental implant suprastructure, permanent, preformed
Primary Device ID00889024020696
NIH Device Record Key88028083-a577-4334-b291-972262c71367
Commercial Distribution StatusIn Commercial Distribution
Brand NameZimmer ZFX Component
Version Model NumberZFX09000642
Company DUNS103167086
Company NameZIMMER DENTAL INC.
Device Count1
DM Exempttrue
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

Phone+1(800)854-7019
Emailzimmer.consumerrelations@zimmer.com
Phone+1(800)854-7019
Emailzimmer.consumerrelations@zimmer.com
Phone+1(800)854-7019
Emailzimmer.consumerrelations@zimmer.com
Phone+1(800)854-7019
Emailzimmer.consumerrelations@zimmer.com
Phone+1(800)854-7019
Emailzimmer.consumerrelations@zimmer.com
Phone+1(800)854-7019
Emailzimmer.consumerrelations@zimmer.com
Phone+1(800)854-7019
Emailzimmer.consumerrelations@zimmer.com
Phone+1(800)854-7019
Emailzimmer.consumerrelations@zimmer.com
Phone+1(800)854-7019
Emailzimmer.consumerrelations@zimmer.com
Phone+1(800)854-7019
Emailzimmer.consumerrelations@zimmer.com
Phone+1(800)854-7019
Emailzimmer.consumerrelations@zimmer.com
Phone+1(800)854-7019
Emailzimmer.consumerrelations@zimmer.com
Phone+1(800)854-7019
Emailzimmer.consumerrelations@zimmer.com
Phone+1(800)854-7019
Emailzimmer.consumerrelations@zimmer.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100889024020696 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

NHAABUTMENT, IMPLANT, DENTAL, ENDOSSEOUS

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00889024020696]

Moist Heat or Steam Sterilization


[00889024020696]

Moist Heat or Steam Sterilization


[00889024020696]

Moist Heat or Steam Sterilization


[00889024020696]

Moist Heat or Steam Sterilization


[00889024020696]

Moist Heat or Steam Sterilization


[00889024020696]

Moist Heat or Steam Sterilization


[00889024020696]

Moist Heat or Steam Sterilization


[00889024020696]

Moist Heat or Steam Sterilization


[00889024020696]

Moist Heat or Steam Sterilization


[00889024020696]

Moist Heat or Steam Sterilization


[00889024020696]

Moist Heat or Steam Sterilization


[00889024020696]

Moist Heat or Steam Sterilization


[00889024020696]

Moist Heat or Steam Sterilization


[00889024020696]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number5
Public Version Date2019-11-08
Device Publish Date2015-10-23

On-Brand Devices [Zimmer ZFX Component]

00889024344433ZFX09000628
00889024344426ZFX09000627
00889024020696ZFX09000642
00889024020689ZFX09000641
00889024020306VENEERZR
00889024020283VENEERTI
00889024020276VENEERPMMA
00889024020252VENEERCOCR
00889024018723TELEZR
00889024018709TELETI
00889024018693TELECOCR
00889024015623MHLASP
00889024015593INLAYZR
00889024015579INLAYTI
00889024015548INLAYCOCR
00889024014831FBRIDGEZR
00889024014817FBRIDGETI
00889024014787FBRIDGECOCR
00889024014541CROWNZR
00889024014527CROWNTI
00889024014510CROWNPMMA
00889024014497CROWNEMAX
00889024014480CROWNCOCR
00889024014473COPINGZR
00889024014459COPINGTI
00889024014428COPINGEMAX
00889024014411COPINGCOCR
00889024014404COPANAZR
00889024014381COPANATI
00889024014350COPANAEMAX
00889024014343COPANACOCR
00889024015562INLAYPMMA
00889024014800FBRIDGEPMMA
00889024014442COPINGPMMA
00889024014374COPANAPMMA

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