Mast Biosurgery USA, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Mast Biosurgery USA, Inc. - FDA 510(k) Cleared Devices
4
Total
3
Cleared
0
Denied
Mast Biosurgery USA, Inc. has 3 FDA 510(k) cleared medical devices. Based in San Diego, US.
Historical record: 3 cleared submissions from 2005 to 2010. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Mast Biosurgery USA, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Mast Biosurgery USA, Inc.
4 devices
Cleared
Jan 07, 2010
CARDIO-WRAP
Cardiovascular
303d
Cleared
Mar 07, 2007
SURGI-WRAP MAST TENDON SHEET
General & Plastic Surgery
90d
Cleared
Sep 21, 2006
SURGI-WRAP MAST BIORESORBABLE SHEET
General & Plastic Surgery
114d
Cleared
May 27, 2005
SURGI-WRAP MAST BIORESORBABLE SHEET
General & Plastic Surgery
106d