Bioform, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
4
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K033398LARYNGEAL AUGMENTATION IMPLANTDecember 12, 2003
K030682CALCIUM HYDROXYLAPATITE IMPLANT, ICC AND 0.5CC, MODELS 8038-3, 8037-3June 27, 2003
K013243COAPTITE LARYNGEAL AUGMENTATION SYSTEM 1CC & O.5CC, MODELS 0008021-1, 0008022-1January 9, 2002
K012955COAPTITE TISSUE MARKER AND COAPTITE FN TISSUE MARKEROctober 22, 2001