Bioform, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Bioform, Inc. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Bioform, Inc. has 4 FDA 510(k) cleared medical devices. Based in Franksville, US.
Historical record: 4 cleared submissions from 2001 to 2003. Primary specialty: Ear, Nose, Throat.
Browse the FDA 510(k) cleared devices submitted by Bioform, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Bioform, Inc.
4 devices
Cleared
Dec 12, 2003
LARYNGEAL AUGMENTATION IMPLANT
Ear, Nose, Throat
49d
Cleared
Jun 27, 2003
CALCIUM HYDROXYLAPATITE IMPLANT, ICC AND 0.5CC, MODELS 8038-3, 8037-3
Dental
114d
Cleared
Jan 09, 2002
COAPTITE LARYNGEAL AUGMENTATION SYSTEM 1CC & O.5CC, MODELS 0008021-1, 0008022-1
Ear, Nose, Throat
103d
Cleared
Oct 22, 2001
COAPTITE TISSUE MARKER AND COAPTITE FN TISSUE MARKER
General & Plastic Surgery
48d