Coil

FDA Filings

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

FDA Registration(s)
Registration Number3003966756
FEI Number3003966756
NameWIPAC LTD COIL
Owner & OperatorCoil
Contact AddressWIPAC LTD, COIL LONDON ROAD
BUCKINGHAM GB-BKM Buckinghamshire MK181BH GB
Official Correspondent
  • Andrew J Green
  • 044-1753-610825-x
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration AddressLONDON ROAD
BUCKINGHAM Buckinghamshire, MK181BH GB
Establishment TypeManufacture Medical Device



FDA Owner/Operator Registration

FDA Filings

Device
Company
DeviceDate
WIPAC LTD COIL [Coil]
Frame spectacle2015-04-27
WIPAC LTD COIL [Coil]
Sunglasses2015-04-27
WIPAC LTD COIL [Coil]
Lens Spectacle2015-04-27
WIPAC LTD COIL [Coil]
Spectacle Magnifying2015-04-27
COIL
PATHFINDER SUNGLASSES1997-05-29

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