Imactis

FDA Filings

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

FDA Registration(s)
Registration Number3015060224
FEI Number3015060224
NameCatherine Gloster
Owner & OperatorIMACTIS
Contact Address20 rue du Tour de l'eau
Saint-Martin d'h?res FR-38 Isere 38400 FR
Official Correspondent
  • Mady BATAILH
  • 33-4-580055-80
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address577 North Hope Ave
Santa Barbara, CA 93110 US
Establishment TypeManufacture Medical Device

FDA Owner/Operator Registration

FDA Filings

Device
Company
DeviceDate
IMACTIS
 IMACTIS® MA-J000972019-01-08
IMACTIS
 IMACTIS® MA-J020002019-01-07
IMACTIS
 IMACTIS® 2019-01-07
IMACTIS
 IMACTIS® MA-J00099_US2019-01-07
IMACTIS
 IMACTIS® MA-I101002019-01-07
IMACTIS
 IMACTIS® 2019-01-07
IMACTIS
 IMACTIS® 2019-01-07
Catherine Gloster [IMACTIS]
Imactis Mobile Cart2018-12-06
Catherine Gloster [IMACTIS]
USMAN MAGNETIC NAVIGATION STATION2018-11-23
Catherine Gloster [IMACTIS]
IMACTIS CT-Navigation system2018-11-23

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