Bioderm, Inc.
FDA 510(k) & PMA Approved Devices — 14 products
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Total Devices14
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K990955 | MODIFICATION OF:BIODERM FOAM WOUND DRESSING | KMF | 1999-05-18 | View |
| 510(k) | K982778 | BIODERM FOAM WOUND DRESSING | KMF | 1998-10-21 | View |
| 510(k) | K982939 | BTF THIN FILM WOUND DRESSING | MGP | 1998-10-13 | View |
| 510(k) | K980451 | BIODERM CALCIUM ALGINATE DRESSING | KMF | 1998-04-09 | View |
| 510(k) | K973429 | BIODERM FOAM WOUND DRESSING | KMF | 1997-12-01 | View |
| 510(k) | K963950 | BIODERM EID MALE EXTERNAL INCONTINENCE DEVICE | EXI | 1997-01-10 | View |
| 510(k) | K963602 | BIODERM PVP FOAM WOUND DRESSING | KMF | 1996-10-30 | View |
| 510(k) | K951166 | BIODERM MEDICAL HYDROGEL ISLAND DRESSING | NAE | 1995-06-21 | View |
| 510(k) | K951842 | BIODERM MEDICAL TRANSPARENT FILM DRESSING | MGP | 1995-06-12 | View |
| 510(k) | K950685 | BIODERM MEDICAL HYDROCOLLOID WOUND DRESSING | KMF | 1995-06-09 | View |
| 510(k) | K950619 | BIODERM MEDICAL FOAM WOUND DRESSING | KMF | 1995-04-25 | View |
| 510(k) | K946292 | BIODERM MEDICAL COMPOSITE WOUND DRESSING | MGP | 1995-02-06 | View |
| 510(k) | K871327 | D.R.P. THREE STEP WOUND DRESSING | FRO | 1987-11-09 | View |
| 510(k) | K870352 | RUBYCELL(TM) SYNTHETIC ISLAND DRESSING | FRO | 1987-02-26 | View |
No matching devices.
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