Sentreheart Inc

FDA Filings

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

FDA Registration(s)
Registration Number3005802238
FEI Number3006482885
NameSENTREHEART INC.
Owner & OperatorATRICURE, INC.
Contact Address7555 Innovation Way --
Mason OH 45040 US
Official Correspondent
  • John S Ehlert
  • x-513-6448220-x
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address300 Saginaw Dr
Redwood City, CA 94063 US
Establishment TypeManufacture Medical Device



FDA Filings

Device
Company
DeviceDate
SENTREHEART, INC
EndoCATH 20062023-12-04
SENTREHEART, INC
Tensure 80022020-05-06
SENTREHEART, INC
SureCUT 50012020-02-06
SENTREHEART INC. [ATRICURE, INC.]
LARIAT RS Suture Delivery Device2019-11-07
SENTREHEART INC. [ATRICURE, INC.]
LARIAT RS Suture Delivery Device2019-11-07
SENTREHEART INC. [ATRICURE, INC.]
LARIAT+ Suture Delivery Device2019-11-07
SENTREHEART INC. [ATRICURE, INC.]
LARIAT+ Suture Delivery Device2019-11-07
SENTREHEART INC. [ATRICURE, INC.]
LARIAT Suture Delivery Device; SofTIP Guide Cannula2019-11-07
SENTREHEART INC. [ATRICURE, INC.]
LARIAT Suture Delivery Device; SofTIP Guide Cannula2019-11-07
SENTREHEART INC. [ATRICURE, INC.]
FindrWirz Guide Wire System2019-11-07
SENTREHEART INC. [ATRICURE, INC.]
EndoCATH Occlusion Balloon2019-11-07
SENTREHEART INC. [ATRICURE, INC.]
TenSURE Suture Puller2019-11-07
SENTREHEART INC. [ATRICURE, INC.]
SureCUT Suture Cutter2019-11-07
SentreHEART, Inc.
LARIAT RS Suture Delivery Device2015-11-25
SENTREHEART INC.
LARIAT Sulture Delivery Device2014-09-12
SENTREHEART INC.
LARIAT II SUTURE DELIVERY DEVICE2009-05-06
SENTREHEART INC.
FINDRWIRZ GUIDE WIRE SYSTEM2008-08-11
SENTREHEART INC.
OCCLUSION BALLOON CATHETER2008-02-08

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