FDA.reportPublic FDA data

MEDICAL MURRAY, INC.

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
14247783003473227MEDICAL MURRAY, INC.1N2026-01-01540 Capital Drive Suite 150 Lake Zurich IL US 60047
30113243933011324393MEDICAL MURRAY, INC.1N2020-04-258531 Steele Creek Place Drive Suite D Charlotte NC US 28273

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
1778851379907187K170675Graftgun Universal Graft Delivery SystemFMF2017-07-19
1778851304000282K162429ZipE Knotless Tissue Repair and Attachment DevicesMAI2017-03-13
200541866409558K162110CORGRIP NG/NI Tube Retention SystemKNT2016-09-15
200541341683560K153488Occlusion Perfusion CatheterQEY2016-02-25
200541778064579K152474Avitus Bone HarvesterKNW2015-10-23
200541152263439K150951aeris Balloon Dialation CatheterKTI2015-06-25
200541391114494K133599CORGRIPKNT2014-03-26
200541358941793K120025SURGIMESH XB - SKIRTEDFTL2012-06-26
200542016009397K072974SURGIMESH XBFTL2008-08-18
200541564009377K061445SURGIMESH WNFTL2007-02-01
200541407375533
1778851630559798
1778851720413645
200541173987137
200541341045463
200541393140127
200541424894349
200541564676759
200541855070439
200542007522512

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
FTL32012-06-26
KNT22016-09-15
FMF12017-07-19
MAI12017-03-13
QEY12016-02-25
KNW12015-10-23
KTI12015-06-25