Bionime Coporation is one of 13040 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Bionime Coporation - FDA 510(k) Cleared Devices
Recent clearances: Rightest Blood Glucose Monitoring System GM700, Rightest Blood Glucose Monitoring System GM650, GE200 Blood Glucose Monitoring System, and GE300 Talking Blood Glucose Monitoring System, GE333 Blood Glucose Monitoring System, RIGHTEST DIABETES MANAGEMENT SOFTWARE AND ADAPTER (EXISTING CLEARED K113007),RIGHTEST NEW ADAPTERS-3,GE DIABETES MANAGEM
3
Total
3
Cleared
0
Denied
Bionime Coporation has 3 FDA 510(k) cleared medical devices. Based in Mission Viejo, US.
Historical record: 3 cleared submissions from 2014 to 2015. Primary specialty: Chemistry.
Browse the FDA 510(k) cleared devices submitted by Bionime Coporation Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Ivdd Regulatory Consultant as regulatory consultant.
FDA 510(k) Regulatory Record - Bionime Coporation
3 devices