Bioform Medical, Inc.
FDA 510(k) & PMA Approved Devices — 3 products
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Total Devices3
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K081729 | MODIFICATION TO GFX NERVE ABLATION SYSTEM | GXD | 2008-08-07 | View |
| 510(k) | K070090 | RADIESSE LARYNGEAL IMPLANT | MIX | 2007-03-01 | View |
| 510(k) | K060815 | JULIESSE INJECTABLE LARYNGEAL AUGMENTATION IMPLANT | MIX | 2006-04-18 | View |
No matching devices.
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