Belega, Inc. is one of 79 FDA 510(k) medical device manufacturers from Japan in the dataset, ranked by real submission volume.
Belega, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Beagank 4T Plus
1
Total
1
Cleared
0
Denied
Belega, Inc. has 1 FDA 510(k) cleared medical devices. Based in Kita-Ku, JP.
Last cleared in 2023. Active since 2023. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Belega, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Ken Block Consulting Co., Ltd. as regulatory consultant.
FDA 510(k) Regulatory Record - Belega, Inc.
1 devices