Bioform Medical, Inc.
3 FDA 510(k) clearances · Manufacturer
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| Record | Firm | Date |
|---|---|---|
| MODIFICATION TO GFX NERVE ABLATION SYSTEM (K081729) | Bioform Medical, Inc. | 2008-08-07 |
| RADIESSE LARYNGEAL IMPLANT (K070090) | Bioform Medical, Inc. | 2007-03-01 |
| JULIESSE INJECTABLE LARYNGEAL AUGMENTATION IMPLANT (K060815) | Bioform Medical, Inc. | 2006-04-18 |
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