Joe Pichon

FDA Filings

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

FDA Registration(s)
Registration Number2205
FEI Number2205
NameJoe Pichon
Owner & OperatorRENISHAW PLC
Contact AddressNEW MILLS WOTTON-UNDER-EDGE
GLOUCESTERSHIRE GB-GLS Gloucestershire GL12 8JR GB
Official Correspondent
  • Jim Baker
  • 44-145-3524395-x
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address1001 Wesemann Drive
West Dundee, IL 60118 US
Establishment Type
  • Develop Specifications But Do Not Manufacture At This Facility
  • Manufacture Medical Device



FDA Filings

Device
Company
DeviceDate
Joe Pichon [RENISHAW PLC]
neuro inspire2017-10-18
Joe Pichon [RENISHAW PLC]
Ti DG1 Titanium Powder Ti6-4-GD232017-05-11

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