Medtrax Industries, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Medtrax Industries, Inc. - FDA 510(k) Cleared Devices
6
Total
2
Cleared
0
Denied
Medtrax Industries, Inc. has 2 FDA 510(k) cleared medical devices. Based in Longwood, US.
Historical record: 2 cleared submissions from 1993 to 1994. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Medtrax Industries, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Medtrax Industries, Inc.
6 devices
Cleared
Apr 14, 1994
PLAIN GAUZE DRESSING
General & Plastic Surgery
57d
Cleared
Mar 31, 1994
WET DRESSING
General & Plastic Surgery
43d
Cleared
Mar 30, 1994
PETROLATUM DRESSING
General & Plastic Surgery
42d
Cleared
Mar 30, 1994
XEROFORM PETROLATUM DRESSING
General & Plastic Surgery
42d
Cleared
Oct 28, 1993
SURE-ADAPT NON-ADHERING DRESSING
General & Plastic Surgery
73d
Cleared
May 12, 1993
MEDTRAX PACKING STRIP
General & Plastic Surgery
154d