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Bioderm, Inc.

14 FDA 510(k) clearances · Manufacturer

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RecordFirmDate
MODIFICATION OF:BIODERM FOAM WOUND DRESSING (K990955)Bioderm, Inc.1999-05-18
BIODERM FOAM WOUND DRESSING (K982778)Bioderm, Inc.1998-10-21
BTF THIN FILM WOUND DRESSING (K982939)Bioderm, Inc.1998-10-13
BIODERM CALCIUM ALGINATE DRESSING (K980451)Bioderm, Inc.1998-04-09
BIODERM FOAM WOUND DRESSING (K973429)Bioderm, Inc.1997-12-01
BIODERM EID MALE EXTERNAL INCONTINENCE DEVICE (K963950)Bioderm, Inc.1997-01-10
BIODERM PVP FOAM WOUND DRESSING (K963602)Bioderm, Inc.1996-10-30
BIODERM MEDICAL HYDROGEL ISLAND DRESSING (K951166)Bioderm, Inc.1995-06-21
BIODERM MEDICAL TRANSPARENT FILM DRESSING (K951842)Bioderm, Inc.1995-06-12
BIODERM MEDICAL HYDROCOLLOID WOUND DRESSING (K950685)Bioderm, Inc.1995-06-09
BIODERM MEDICAL FOAM WOUND DRESSING (K950619)Bioderm, Inc.1995-04-25
BIODERM MEDICAL COMPOSITE WOUND DRESSING (K946292)Bioderm, Inc.1995-02-06
D.R.P. THREE STEP WOUND DRESSING (K871327)Bioderm, Inc.1987-11-09
RUBYCELL(TM) SYNTHETIC ISLAND DRESSING (K870352)Bioderm, Inc.1987-02-26

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