Bionix Development Corporation - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Bionix Development Corporation has 1 FDA 510(k) cleared medical devices. Based in Toledo, US.
Historical record: 1 cleared submissions from 2018 to 2018. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Bionix Development Corporation Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Bionix Development Corporation
1 devices