BioDerm, Inc.
3 FDA 510(k) clearances · Recalling firm
| Record | Firm | Date |
|---|---|---|
| BioDerm Liberty 3.0 External Male Catheter Specialty Type with integral collection chamber recall (Z-1742-2014) | BioDerm, Inc. | 2014-06-10 |
| BioDerm Liberty Pouch Clean & Dry External Male Catheter Specialty Type with integral coll recall (Z-1743-2014) | BioDerm, Inc. | 2014-06-10 |
| BioDerm Safe n' Dry 21006 (Component: SKIN-PREP Protective wipes). The recalled wipes are recall (Z-1744-2014) | BioDerm, Inc. | 2014-06-10 |
Track BioDerm, Inc. automatically
Every clearance here is in the API, with alerts when new ones post.