Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
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.
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact