Proteor Usa

FDA Filings

This page includes the latest FDA filings for Proteor Usa. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)
Registration Number3008584163
FEI Number3008584163
NamePROTEOR USA
Owner & OperatorCompliance Insight, Inc.
Contact Address1236 West Southern Avenue Suite 101
Tempe AZ 85282 US
Official Correspondent
  • Dia P Hill
  • x-513-8603512-304
Registration Status1
Initial ImporterY
Registration Expiration2020-04-25
Registration Address1236 W SOUTHERN AVE STE 101
Tempe, AZ 85282 US
Establishment TypeRepack or Relabel Medical Device



FDA Filings

Device
Company
DeviceDate
PROTEOR USA [Compliance Insight, Inc.]
Aflex2019-01-31
PROTEOR USA [Compliance Insight, Inc.]
Keasy2019-01-31
PROTEOR USA [Compliance Insight, Inc.]
Symphony Knee2019-01-31
PROTEOR USA [Compliance Insight, Inc.]
Easy Ride Hydeal Knee HydraCadence Knee HyTrek Matik Knee2019-01-31
PROTEOR USA [Compliance Insight, Inc.]
Allux (Distributor only)2019-01-31
PROTEOR USA [Compliance Insight, Inc.]
RUSH:HiPro HiProEVAQ8 HiProH2O Chopart ROVER kid; RUSH RAMPAGE:EVAQ8 LP LP H2O; RUSH ROGUE:EVAQ8 H2O (Manufacturer)2010-05-05
PROTEOR USA [Compliance Insight, Inc.]
Easy Run Blade (Repackager/ Relabeler)2010-05-05
PROTEOR USA [Compliance Insight, Inc.]
DynaCity DynaStar Foot DynaStep Foot DynaTrek Gery Foot (Repackager/ Relabeler)2010-05-05

Related Finance Registrations
U.S. Import Records [external site]
Import IDShipmentCargo DescriptionQuantity
20200130188FOS Sur Mer,France -> Long Beach, CaliforniaORTHOPEDIC APPLIANCES10 PKG
201909219400FOS Sur Mer,France -> Long Beach, CaliforniaORTHOPEDIC APPLIANCES10 PKG

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