Dynarex Corporation is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Dynarex Corporation - FDA 510(k) Cleared Devices
Recent clearances: Dynarex Three-Way Stopcock
8
Total
8
Cleared
0
Denied
Dynarex Corporation has 8 FDA 510(k) cleared medical devices. Based in Orangeburg, US.
Historical record: 8 cleared submissions from 2008 to 2018.
Browse the FDA 510(k) cleared devices submitted by Dynarex Corporation Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Dynarex Corporation
8 devices
Cleared
Mar 14, 2018
Dynarex Three-Way Stopcock
General Hospital
230d
Cleared
Oct 03, 2016
Dynarex Xeroform Petrolatum Dressing
General & Plastic Surgery
361d
Cleared
Sep 01, 2015
Dynarex Eye Cups
Ophthalmic
82d
Cleared
Jun 07, 2011
DYNAREX INTERMITTENT CATHETERS, MALE, FEMALE, PEDIATRIC
Gastroenterology & Urology
231d
Cleared
Feb 16, 2011
DYNAREX ULTRASOUND GEL
Radiology
155d
Cleared
Dec 18, 2009
DYNAREX STERILE LUBRICATING JELLY
General Hospital
127d
Cleared
Jan 09, 2009
DYNAREX ENTERAL DELIVERY PUMP SET WITH SPIKE (1000ML), DYNAREX ENTERAL...
Gastroenterology & Urology
102d
Cleared
Sep 12, 2008
DYNAREX/TILLOTSON NON-STERILE POWDER FREE BLUE NITRILE PATIENT EXAM GLOVE FOR...
General Hospital
100d