Recticel Corby

FDA Filings

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

FDA Registration(s)
Registration Number3009222742
FEI Number3009222742
NameRECTICEL CORBY
Owner & OperatorRECTICEL CORBY
Contact AddressManton Road, Earlstrees Ind Estate
CORBY GB-NTH Northamptonshire NN17 4JL GB
Official Correspondent
  • Michelle Cunningham
  • 44-536-402345-x
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration AddressManton Road, Earlstrees Ind Estate
CORBY Northamptonshire, NN17 4JL GB
Establishment TypeManufacture Medical Device for Another Party (Contract Manufacturer)



FDA Filings

Device
Company
DeviceDate
RECTICEL CORBY
Laryngofoam2016-07-25
RECTICEL CORBY
Buchanan2016-07-25
RECTICEL CORBY
Buchanan DeltaNex2016-07-25

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