Interpore Cross I N T L L C

FDA Filings

This page includes the latest FDA filings for Interpore Cross I N T L L C. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)
Registration Number2029012
FEI Number1000160576
NameInterpore Cross International, LLC
Owner & OperatorINTERPORE CROSS INTL.
Contact Address181 TECHNOLOGY DR. --
Irvine CA 92618 US
Official Correspondent
  • PHILIP - MELLINGER
  • x-949-4533200-x
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address181 Technology Drive, Suite 100
IRVINE, CA 92618 US
Establishment TypeManufacture Medical Device for Another Party (Contract Manufacturer)



FDA Filings

Device
Company
DeviceDate
Interpore Cross International, LLC [INTERPORE CROSS INTL.]
Equivabone2018-01-25
Interpore Cross International, LLC [INTERPORE CROSS INTL.]
Equivabone2018-01-25
Interpore Cross International, LLC [INTERPORE CROSS INTL.]
PrimaGen Syringes2017-10-12
Interpore Cross International, LLC [INTERPORE CROSS INTL.]
Mimix2015-03-17
Interpore Cross International, LLC [INTERPORE CROSS INTL.]
Mimix QS2015-03-17
Interpore Cross International, LLC [INTERPORE CROSS INTL.]
Otomimix2014-06-04
Interpore Cross International, LLC [INTERPORE CROSS INTL.]
Calcigen S2014-06-04
Interpore Cross International, LLC [INTERPORE CROSS INTL.]
RegenerOss Allograft Plus Mineralized2012-01-24
Interpore Cross International, LLC [INTERPORE CROSS INTL.]
InterGro DBM, StaGraft DBM, AlloGenix DBM2009-12-17
Interpore Cross International, LLC [INTERPORE CROSS INTL.]
InterGro DBM, StaGraft DBM, AlloGenix DBM2009-12-17
Interpore Cross International, LLC [INTERPORE CROSS INTL.]
InterGro DBM, StaGraft DBM, AlloGenix DBM2009-12-17
Interpore Cross International, LLC [INTERPORE CROSS INTL.]
Pro Osteon 500R w/ BMA2007-12-05
Interpore Cross International, LLC [INTERPORE CROSS INTL.]
Pro Osteon 200R2007-12-05

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