Dynarex Corp. is one of 5576 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Dynarex Corp. - FDA 510(k) Cleared Devices
Recent clearances: DYNAREX CPR SHIELD WITH ONE WAY VALVE AND BARRIER FILTER, MODEL 4921, DYNAREX VAGINAL SPECULA 4900, MODELS 4911-SMALL, 4912-MEDIUM, 4913-LARGE, DYNAREX IODOFORM PACKING STRIPS, MODELS 3411, 3412, 3413, 3414
19
Total
18
Cleared
0
Denied
Dynarex Corp. has 18 FDA 510(k) cleared medical devices. Based in Brewster, US.
Historical record: 18 cleared submissions from 1986 to 2005. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Dynarex Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Dynarex Corp.
19 devices
Cleared
Dec 22, 2005
DYNAREX CPR SHIELD WITH ONE WAY VALVE AND BARRIER FILTER, MODEL 4921
Anesthesiology
83d
Cleared
Nov 09, 2005
DYNAREX VAGINAL SPECULA 4900, MODELS 4911-SMALL, 4912-MEDIUM, 4913-LARGE
Obstetrics & Gynecology
76d
Cleared
Oct 17, 2002
DYNAREX IODOFORM PACKING STRIPS, MODELS 3411, 3412, 3413, 3414
General & Plastic Surgery
421d
Cleared
Mar 06, 2002
TOWEL DRAPE, MODELS 4409, 4410
General Hospital
183d
Cleared
Nov 28, 2001
DYNAREX UMBILICAL CORD LAMP, MODELS 6833 AND 6833-B
Obstetrics & Gynecology
90d
Cleared
Jul 15, 1999
DYNAREX DRAIN SPONGE
General & Plastic Surgery
58d
Cleared
Jul 15, 1999
DYNAREX NON-WOVEN SPONGE
General & Plastic Surgery
58d
Cleared
Dec 11, 1998
DYNAREX TRACHEOSTOMY SPONGE
General & Plastic Surgery
79d
Cleared
Apr 01, 1996
DYNAREX NON-WOVEN SPONGE
General & Plastic Surgery
66d
Cleared
May 09, 1995
DYNAREX GAUZE SPONGE
General & Plastic Surgery
29d
Cleared
Dec 22, 1993
DYNAREX GAUZE SPONGE OR PADS
General & Plastic Surgery
168d
Cleared
Jan 11, 1993
DYNAREX SUCTION CATHETERS & KITS
Anesthesiology
213d