Sunbio, Inc. is one of 351 FDA 510(k) medical device manufacturers from South Korea in the dataset, ranked by real submission volume.
Sunbio, Inc. - FDA 510(k) Cleared Devices
Recent clearances: MucoPEG
1
Total
1
Cleared
0
Denied
Sunbio, Inc. has 1 FDA 510(k) cleared medical devices. Based in Gunpo-Si, KR.
Historical record: 1 cleared submissions from 2019 to 2019. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Sunbio, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Emergo by UL as regulatory consultant.
FDA 510(k) Regulatory Record - Sunbio, Inc.
1 devices