Dumex Medical Surgical Products, Ltd. is one of 208 FDA 510(k) medical device manufacturers from Canada in the dataset, ranked by real submission volume.
Dumex Medical Surgical Products, Ltd. - FDA 510(k) Cleared Devices
13
Total
10
Cleared
0
Denied
Dumex Medical Surgical Products, Ltd. has 10 FDA 510(k) cleared general & plastic surgery devices. Based in Toronto, Orntario, CA.
Historical record: 10 cleared submissions from 1994 to 2000.
Browse the complete list of FDA 510(k) cleared general & plastic surgery devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Dumex Medical Surgical Products, Ltd.
13 devices
Cleared
Apr 20, 2000
STERILE WATER & STERILE 0.9% SODIUM CHLORIDE
General Hospital
251d
Cleared
Nov 23, 1999
STERILE HYDROGEL
General & Plastic Surgery
64d
Cleared
Apr 14, 1999
DUMEX IODOFORM PACKING STRIP
General & Plastic Surgery
70d
Cleared
Jun 26, 1998
THALAFIX NATURAL SEA SALT DRESSING
General & Plastic Surgery
116d
Cleared
May 20, 1998
DUMEX PAK-ITS COTTON GAUZE PACKING IMPREGNATED WITH HYDROGEL
General & Plastic Surgery
76d
Cleared
May 11, 1998
DUMEX PAK-ITS NON-WOVEN DRESSING IMPREGNATED SITH SODIUM CHLORIDE (HYPERTONIC)
General & Plastic Surgery
67d
Cleared
May 04, 1998
DUMEX PAK-ITS-ABSORBASALT COTTON GAUZE PACKING
General & Plastic Surgery
63d
Cleared
Apr 29, 1998
DUMEX PAK-ITS WOVEN RIBBON PACKING
General & Plastic Surgery
58d
Cleared
Apr 29, 1996
DUPAD, DUPAD W/ABDOM. PAD, DUMEX ABDOM. PAD, COMBO DRESSING ROLL/COMBINE...
General & Plastic Surgery
61d
Cleared
Mar 01, 1995
DUMEX WET DRESSINGS
General & Plastic Surgery
47d
Cleared
Jan 24, 1995
DUTEX GAUZE BANDAGE
General & Plastic Surgery
33d
Cleared
Jan 11, 1995
DUFLEX CONFORMING BANDAGE (STERILE/NON-STERILE)
General & Plastic Surgery
43d
Cleared
Apr 21, 1994
DUPAQUE SPONGE
General & Plastic Surgery
38d