Bioform, Inc.
Bioform, Inc. appears in FDA public data with 0 recalls, 4 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on December 12, 2003.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 4
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K033398 | LARYNGEAL AUGMENTATION IMPLANT | December 12, 2003 |
| K030682 | CALCIUM HYDROXYLAPATITE IMPLANT, ICC AND 0.5CC, MODELS 8038-3, 8037-3 | June 27, 2003 |
| K013243 | COAPTITE LARYNGEAL AUGMENTATION SYSTEM 1CC & O.5CC, MODELS 0008021-1, 0008022-1 | January 9, 2002 |
| K012955 | COAPTITE TISSUE MARKER AND COAPTITE FN TISSUE MARKER | October 22, 2001 |