Mc3 Inc

FDA Filings

This page includes the latest FDA filings for Mc3 Inc. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)
Registration Number3011468686
FEI Number3011468686
NameMC3 INC.
Owner & OperatorMC3 Inc.
Contact Address2555 Bishop Circle West
Dexter MI 48130 US
Official Correspondent
  • Martha J RUMFORD
  • x-734-9959089-232
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address2555 Bishop Cir W
Dexter, MI 48130 US
Establishment Type
  • Manufacture Medical Device
  • Manufacture Device in the United States for Export Only

FDA Filings

Device
Company
DeviceDate
MC3 Incorporated
Nautilus Smart ECMO Module2020-04-09
MC3 INC.
MC3 Nautilus Smart ECMO Module with Balance Biosurface2020-04-09
MC3 INC.
MC3 Nautilus ECMO Oxygenator with Balance Biosurface2020-04-09
MC3 INC.
Nautilus ECMO Oxygenator with Balance Biosurface2019-10-12
MC3 INC.
MC3 Vascular Access Kit2019-04-12
MC3 Incorporated
MC3 Vascular Access Kit 210302018-10-29
MC3 INC.
Crescent(tm) Jugular Dual Lumen Catheter2018-07-24
MC3 Incorporated
MC3 Jugular Dual Lumen Catheter2018-07-16
MC3 Incorporated
MC3 QuickFlow Dual Lumen Catheter2017-11-16
MC3 INC.
Soft-Flow Extended Aortic Cannula2016-09-06
MC3 INC.
Soft-Flow Aortic Cannula2016-08-12

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