Interpore Cross International, LLC

Matched from indexed company URL: INTERPORE CROSS INTERNATIONAL

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
20290121000160576Interpore Cross International, LLC1N2020-04-25181 Technology Drive, Suite 100 IRVINE CA US 92618

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
343701127411961K990290CRANIOFACIAL CALCIUM PHOSPHATE CERAMIC BONE FILLERGXP1999-11-18
343701639712221K140710BIOMET GRAFT DELIVERY SYRINGESFMF2014-09-04
343701330744794K113645REGENEROSS ALLOGRAFT PLUS MINERLIZEDNUN2012-01-20
343701849195967K101557GAMMA-BSM, BETA-BSM, EQUIVABONE, CARIGENMQV2010-07-01
343701278768912K082793INTERGRO DBMMQV2009-04-02
343701450388216K063346PRO OSTEON 500RMQV2007-04-18
343701088022426K042516OTOMIMIXNEA2004-11-08
343701174887313K023718QUICKSET MIMIX BONE VOID FILLERGXP2002-12-04
343701311672449K013790CALCIGEN-S BONE VOID FILERMQV2002-06-11
343701282404844K000515PRO OSTEON 200R RESORBABLE BONE GRAFT SUBSTITUTE, MODELS 2RG051, 2RG101, 2RG151, 2RG201, 2RG301, 2RG050, 2RG100, 2RG150,MQV2000-09-15

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
MQV52010-07-01
GXP22002-12-04
FMF12014-09-04
NUN12012-01-20
NEA12004-11-08