Dermaphylyx, Inc. - FDA 510(k) Cleared Devices
9
Total
7
Cleared
0
Denied
Dermaphylyx, Inc. has 7 FDA 510(k) cleared medical devices. Based in Arvada, US.
Historical record: 7 cleared submissions from 1999 to 1999. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Dermaphylyx, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Dermaphylyx, Inc.
9 devices
Cleared
Sep 14, 1999
DERMAPHYLYX SKIN PROTECTORS, PROTECT IT SKIN PROTECTORS
General & Plastic Surgery
68d
Cleared
Aug 12, 1999
DERMAPHYLYX HYDROPHILIC FOAM WOUND DRESSING
General & Plastic Surgery
66d
Cleared
Jul 30, 1999
DERMAPHYLYX FOAM ISLAND DRESSING
General & Plastic Surgery
52d
Cleared
Jul 20, 1999
DERMAPHYLYX CALCIUM ALGINATE WOUND DRESSING
General & Plastic Surgery
71d
Cleared
Jul 20, 1999
DERMAPHYLYX SUPER ABSORBENT FIBER DRESSING
General & Plastic Surgery
71d
Cleared
Jun 28, 1999
DERMAPHYLYX CALCIUM ALGINATE WOUND DRESSING
General & Plastic Surgery
90d
Cleared
May 27, 1999
DERMAPHYLYX FILM WOUND DRESSING AND HEALIAN FILM WOUND DRESSING
General & Plastic Surgery
72d
Cleared
May 27, 1999
DERMAPHYLYX HYDROCOLLOID WOUND DRESSING, HEALIAN HYDROCOLLOID WOUND DRESSING
General & Plastic Surgery
71d
Cleared
Mar 25, 1999
DERMAFLEX WOUND DRESSING, DERMAFLEX FOAM WOUND DRESSING, HEALIAFLEX WOUND...
General & Plastic Surgery
42d