Bioform, Inc.
FDA 510(k) & PMA Approved Devices — 4 products
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Total Devices4
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K033398 | LARYNGEAL AUGMENTATION IMPLANT | MIX | 2003-12-12 | View |
| 510(k) | K030682 | CALCIUM HYDROXYLAPATITE IMPLANT, ICC AND 0.5CC, MODELS 8038-3, 8037-3 | LYC | 2003-06-27 | View |
| 510(k) | K013243 | COAPTITE LARYNGEAL AUGMENTATION SYSTEM 1CC & O.5CC, MODELS 0008021-1, 0008022-1 | KHJ | 2002-01-09 | View |
| 510(k) | K012955 | COAPTITE TISSUE MARKER AND COAPTITE FN TISSUE MARKER | NEU | 2001-10-22 | View |
No matching devices.
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