FDA 510(k) Applications Submitted by BIOFORM, INC.

FDA 510(k) Number Submission Date Device Name Applicant
K033398 10/24/2003 LARYNGEAL AUGMENTATION IMPLANT BIOFORM, INC.
K012955 09/04/2001 COAPTITE TISSUE MARKER AND COAPTITE FN TISSUE MARKER BIOFORM, INC.
K013243 09/28/2001 COAPTITE LARYNGEAL AUGMENTATION SYSTEM 1CC & O.5CC, MODELS 0008021-1, 0008022-1 BIOFORM, INC.
K030682 03/05/2003 CALCIUM HYDROXYLAPATITE IMPLANT, ICC AND 0.5CC, MODELS 8038-3, 8037-3 BIOFORM, INC.


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