Biowy Corporation is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Biowy Corporation - FDA 510(k) Cleared Devices
Recent clearances: Biowy Tym Tube (TT), Biowy PICC Catheter S Kit, Biowy PlCC Catheter
3
Total
3
Cleared
0
Denied
Biowy Corporation has 3 FDA 510(k) cleared medical devices. Based in Lake Forest, US.
Latest FDA clearance: Feb 2024. Active since 2018. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Biowy Corporation Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Biowy Corporation
3 devices