Katy Black

FDA Filings

This page includes the latest FDA filings for Katy Black. 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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