Rex Medical is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Rex Medical - FDA 510(k) Cleared Devices
13
Total
11
Cleared
0
Denied
Rex Medical has 11 FDA 510(k) cleared cardiovascular devices. Based in Great Neck, US.
Historical record: 11 cleared submissions from 2003 to 2012.
Browse the complete list of FDA 510(k) cleared cardiovascular devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Rex Medical
13 devices
Cleared
Jun 01, 2012
CLEANER ROTATIONAL THROMBECTOMY SYSTEM
Cardiovascular
119d
Cleared
May 22, 2012
SPLITWIRE PERCUTANEOUS TRANSLUMINAL ANGIOPLASTY SCORING DEVICE
Cardiovascular
216d
Cleared
Nov 18, 2010
ULTRASTREAM CHRONIC HEMODIALYSIS CATHETER
Gastroenterology & Urology
121d
Cleared
Feb 18, 2010
CLEANER ROTATIONAL THROMBECTOMY SYSTEM (9 MM X 65 CM) AND (9 MM X 120 CM)
Cardiovascular
314d
Cleared
Jun 04, 2009
OPTION VENA CAVA FILTER
Cardiovascular
380d
Cleared
Aug 22, 2007
15.5F HEMO-STREAM HEMODIALYSIS CATHETER SET
Gastroenterology & Urology
92d
Cleared
Aug 04, 2005
INNER-LOCK INTRODUCER SHEATH
Cardiovascular
62d
Cleared
Feb 26, 2004
CLEANER ROTATIONAL THROMBECTOMY SYSTEM KIT
Cardiovascular
22d
Cleared
Dec 16, 2003
CLEANER II ROTATIONAL THROMBECTOMY SYSTEM
Cardiovascular
11d
Cleared
Sep 16, 2003
SHORT INTRODUCER SHEATH
Cardiovascular
27d
Cleared
May 27, 2003
REX MEDICAL CLEANER ROTATIONAL THROMBECTOMY SYSTEM
Cardiovascular
5d
Cleared
Apr 30, 2003
HEMO-STREAM HEMODIALYSIS CATHETER SET
Gastroenterology & Urology
162d
Cleared
Jan 21, 2003
INNER-LOCK LOCKING INTRODUCER SHEATHS
Cardiovascular
202d