Zimmer Knee Creations, Inc.

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30088121733008812173Zimmer Knee Creations, Inc.1N2026-01-0156 E Bell Dr Warsaw IN US 46582

GUDID Contact Samples#

Sampled from matched GUDID device records for this company; this is not an exhaustive company contact directory.

Source GUDID, Product, Phone table
Source GUDIDProductPhoneEmail
00889024205192AccuPort® Cannula - 308.081484-887-8902KC.Customerservice@zimmerbiomet.com

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
1230811045879952K190814AccuFill Bone Substitute MaterialMQV2019-06-10
1230812051955481K133021MIXING SYRINGE SYSTEMFMF2014-01-13
1230812064871745
1230811151182072
1230811465104057
1230811738318045

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
MQV22019-06-10
FMF12014-01-13

PMN#

GUDID#

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