C Pro Direct L T D

FDA Filings

This page includes the latest FDA filings for C Pro Direct L T D. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)
Registration Number3009097552
FEI Number3009097552
NameKaty Black
Owner & OperatorC-Pro Direct Ltd
Contact Address7a The Industrial Estate Enterprise Way
Edenbridge GB-KEN Kent TN8 6HF GB
Official Correspondent
  • Philip G Morris
  • 044-1732-860158-x
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address604 North Parkway Street
Wayland, IA 52654 US
Establishment Type
  • Develop Specifications But Do Not Manufacture At This Facility
  • Manufacture Medical Device



FDA Filings

Device
Company
DeviceDate
Katy Black [C-Pro Direct Ltd]
Abduction Dorsiflexion Mechanism (ADM)2014-03-13
Katy Black [C-Pro Direct Ltd]
Dorsi Ramp2012-04-10

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