Digio2 International Co., Ltd. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Digio2 International Co., Ltd. - FDA 510(k) Cleared Devices
3
Total
3
Cleared
0
Denied
Digio2 International Co., Ltd. has 3 FDA 510(k) cleared medical devices. Based in Flagstaff, US.
Historical record: 3 cleared submissions from 2009 to 2014.
Browse the FDA 510(k) cleared devices submitted by Digio2 International Co., Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Digio2 International Co., Ltd.
3 devices