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/ Biodermis Corp.
Biodermis Corp.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
5
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K003948
EPI-DERM SILICONE GEL SHEETING
January 29, 2001
K992146
SCARAID SILICONE GEL SHEETING
July 30, 1999
K991604
EPI-FOAM SILICONE SHEETING
June 9, 1999
K964047
CRYOSIL SILICONE GEL SHEETING
March 19, 1997
K942156
EPI-DERM SILICONE GEL SHEETING
June 13, 1994