Reflow Medical

FDA Filings

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

FDA Registration(s)
Registration Number3008789872
FEI Number3008789872
NameREFLOW MEDICAL
Owner & OperatorReFlow Medical
Contact Address208 Avenida Fabricante Suite 100
San Clemente CA 92672 US
Official Correspondent
  • Krystal Santiago
  • 1-949-4810399-x
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address208 Avenida Fabricante Suite 100
San Clemente, CA 92672 US
Establishment TypeManufacture Medical Device



FDA Filings

Device
Company
DeviceDate
Reflow Medical
CoraCross2021-05-28
REFLOW MEDICAL
Spex LP Support Catheters2020-04-01
REFLOW MEDICAL
Wingman Crossing Catheters2020-04-01
REFLOW MEDICAL
Wingman Crossing Catheters2020-04-01
REFLOW MEDICAL
Spex Support Catheters2020-04-01
Reflow Medical
SpeX LP Support Catheter2020-03-18
Reflow Medical
Wingman 14, Wingman 14C, Wingman 18, Wingman 352020-02-20
ReFlow Medical
SpeX Support Catheter2020-02-19
REFLOW MEDICAL
Wingman 14C Crossing Catheter2019-10-29
REFLOW MEDICAL
Wingman 35 Crossing Catheter2019-10-29
REFLOW MEDICAL
speX Catheter2018-02-08
REFLOW MEDICAL
Wingman Coronary Crossing Catheter2016-08-22
REFLOW MEDICAL
Wingman Crossing Catheter2015-08-07
REFLOW MEDICAL
Wingman 14 Crossing Catheter2014-12-16
REFLOW MEDICAL
SPEX SUPPORT CATHETER2014-11-05
REFLOW MEDICAL
WINGMAN EXTENDABLE TIP SUPPORT CATHETER2014-09-30
REFLOW MEDICAL
WINGMAN EXTENDABLE TIP SUPPORT CATHETER2013-09-19
REFLOW MEDICAL
WINGMAN EXTENDABLE TIP SUPPORT CATHETER2012-02-08
REFLOW MEDICAL
WINGMAN EXTENDABLE TIP SUPPORT CATHETER2010-08-11

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