Renishaw Mayfield

FDA Filings

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

FDA Registration(s)
Registration Number3009108888
FEI Number3009108888
NameRENISHAW MAYFIELD
Owner & OperatorRenishaw Mayfield
Contact Address31 rue Ampere
Chassieu FR-69 Rhone 69680 FR
Official Correspondent
  • Stephane Vinot
  • 033-4-37238900-x
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address31 rue Ampere
Chassieu Rhone, 69680 FR
Establishment TypeManufacture Medical Device



FDA Filings

Device
Company
DeviceDate
RENISHAW MAYFIELD
neuromate planning station hardware 043.00152024-03-20
RENISHAW MAYFIELD
neuromate - neuroinspire software 001.01232024-03-20
RENISHAW MAYFIELD
Neuromate Planning Station Hardware 001.01302024-03-20
RENISHAW MAYFIELD
neuromate planning station hardware 001.01192024-03-20
RENISHAW MAYFIELD
neuromate neuroinspire software 001.01422024-03-20
RENISHAW MAYFIELD
neuromate tool guide 003.01552022-04-08
RENISHAW MAYFIELD
neuromate tool guide 005.09032022-04-08
RENISHAW MAYFIELD
neuromate tool guide 005.07852022-04-08
RENISHAW MAYFIELD
neuromate tool guide 005.08042022-04-08
RENISHAW MAYFIELD
neuromate tool guide 005.06062022-04-08
RENISHAW MAYFIELD
neuromate tool guide 005.01422022-04-08
RENISHAW MAYFIELD
neuromate tool-holder 2022-04-08
RENISHAW MAYFIELD
neuro|mate® - Adaptation for Fischer ZD frame 2021-03-04
RENISHAW MAYFIELD
NMControl 009.00302019-06-27
RENISHAW MAYFIELD
Neuromate Frameless Gen II2014-07-21

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