Reflow Medical is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Reflow Medical - FDA 510(k) Cleared Devices
Recent clearances: coraCross, speX LP Support Catheter, Wingman 14, Wingman 14C, Wingman 18, Wingman 35
10
Total
10
Cleared
0
Denied
Reflow Medical has 10 FDA 510(k) cleared cardiovascular devices. Based in San Diego, US.
Last cleared in 2021. Active since 2010.
Browse the complete list of FDA 510(k) cleared cardiovascular devices from this manufacturer. Filter by specialty or product code using the sidebar.
1 device has linked clinical trial registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Reflow Medical
10 devices
Cleared
May 28, 2021
coraCross
Cardiovascular
123d
Cleared
Mar 18, 2020
speX LP Support Catheter
Cardiovascular
62d
Cleared
CT
Feb 20, 2020
Wingman 14, Wingman 14C, Wingman 18, Wingman 35
Cardiovascular
59d
Cleared
Feb 19, 2020
speX Support Catheter
Cardiovascular
113d
Cleared
Aug 07, 2015
Wingman Crossing Catheter
Cardiovascular
29d
Cleared
Nov 05, 2014
SPEX SUPPORT CATHETER
Cardiovascular
138d
Cleared
Sep 30, 2014
WINGMAN EXTENDABLE TIP SUPPORT CATHETER
Cardiovascular
111d
Cleared
Sep 19, 2013
WINGMAN EXTENDABLE TIP SUPPORT CATHETER
Cardiovascular
45d
Cleared
Feb 08, 2012
WINGMAN EXTENDABLE TIP SUPPORT CATHETER
Cardiovascular
19d
Cleared
Aug 11, 2010
WINGMAN EXTENDABLE TIP SUPPORT CATHETER
Cardiovascular
75d