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Bioform Medical, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
3
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K081729MODIFICATION TO GFX NERVE ABLATION SYSTEMAugust 7, 2008
K070090RADIESSE LARYNGEAL IMPLANTMarch 1, 2007
K060815JULIESSE INJECTABLE LARYNGEAL AUGMENTATION IMPLANTApril 18, 2006