Biodermis Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Biodermis Corp. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Biodermis Corp. has 5 FDA 510(k) cleared medical devices. Based in Las Vegas, US.
Historical record: 5 cleared submissions from 1994 to 2001. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Biodermis Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Biodermis Corp.
5 devices
Cleared
Jan 29, 2001
EPI-DERM SILICONE GEL SHEETING
General & Plastic Surgery
39d
Cleared
Jul 30, 1999
SCARAID SILICONE GEL SHEETING
General & Plastic Surgery
36d
Cleared
Jun 09, 1999
EPI-FOAM SILICONE SHEETING
General & Plastic Surgery
30d
Cleared
Mar 19, 1997
CRYOSIL SILICONE GEL SHEETING
General & Plastic Surgery
161d
Cleared
Jun 13, 1994
EPI-DERM SILICONE GEL SHEETING
General & Plastic Surgery
41d