Bipad Surgical, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Bipad Surgical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: BiPad Hand Activated, Disposable Bipolar Electrocautery Cords
1
Total
1
Cleared
0
Denied
Bipad Surgical, Inc. has 1 FDA 510(k) cleared medical devices. Based in Point Lookout, US.
Historical record: 1 cleared submissions from 2020 to 2020. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Bipad Surgical, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Accelerated Device Approval Services as regulatory consultant.
FDA 510(k) Regulatory Record - Bipad Surgical, Inc.
1 devices