Bioderm, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Bioderm, Inc. - FDA 510(k) Cleared Devices
14
Total
10
Cleared
0
Denied
Bioderm, Inc. has 10 FDA 510(k) cleared general & plastic surgery devices. Based in Wheaton, US.
Historical record: 10 cleared submissions from 1987 to 1999.
Browse the complete list of FDA 510(k) cleared general & plastic surgery devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Bioderm, Inc.
14 devices
Cleared
May 18, 1999
MODIFICATION OF:BIODERM FOAM WOUND DRESSING
General & Plastic Surgery
57d
Cleared
Oct 21, 1998
BIODERM FOAM WOUND DRESSING
General & Plastic Surgery
75d
Cleared
Oct 13, 1998
BTF THIN FILM WOUND DRESSING
General & Plastic Surgery
53d
Cleared
Apr 09, 1998
BIODERM CALCIUM ALGINATE DRESSING
General & Plastic Surgery
63d
Cleared
Dec 01, 1997
BIODERM FOAM WOUND DRESSING
General & Plastic Surgery
82d
Cleared
Jan 10, 1997
BIODERM EID MALE EXTERNAL INCONTINENCE DEVICE
Gastroenterology & Urology
100d
Cleared
Oct 30, 1996
BIODERM PVP FOAM WOUND DRESSING
General & Plastic Surgery
51d
Cleared
Jun 21, 1995
BIODERM MEDICAL HYDROGEL ISLAND DRESSING
General & Plastic Surgery
99d
Cleared
Jun 12, 1995
BIODERM MEDICAL TRANSPARENT FILM DRESSING
General & Plastic Surgery
53d
Cleared
Jun 09, 1995
BIODERM MEDICAL HYDROCOLLOID WOUND DRESSING
General & Plastic Surgery
115d
Cleared
Apr 25, 1995
BIODERM MEDICAL FOAM WOUND DRESSING
General & Plastic Surgery
74d
Cleared
Feb 06, 1995
BIODERM MEDICAL COMPOSITE WOUND DRESSING
General & Plastic Surgery
41d
Cleared
Nov 09, 1987
D.R.P. THREE STEP WOUND DRESSING
General & Plastic Surgery
220d
Cleared
Feb 26, 1987
RUBYCELL(TM) SYNTHETIC ISLAND DRESSING
General & Plastic Surgery
28d