Dermarx Corp. is one of 6989 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Dermarx Corp. - FDA 510(k) Cleared Devices
Recent clearances: DERMAMEND HYDROGEL GAUZE DRESSING, DERMAMEND FOAM ISLAND DRESSING
4
Total
3
Cleared
0
Denied
Dermarx Corp. has 3 FDA 510(k) cleared medical devices. Based in Denver, US.
Historical record: 3 cleared submissions from 1995 to 1997. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Dermarx Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Dermarx Corp.
4 devices