Biosculpture Technology, Inc. is one of 25823 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Biosculpture Technology, Inc. - FDA 510(k) Cleared Devices
Recent clearances: AIRBRUSH LIPOSCULPTOR SYSTEM
1
Total
1
Cleared
0
Denied
Biosculpture Technology, Inc. has 1 FDA 510(k) cleared medical devices. Based in New York, US.
Historical record: 1 cleared submissions from 2003 to 2003. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Biosculpture Technology, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Entela, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Biosculpture Technology, Inc.
1 devices