Aibiomed, Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Aibiomed, Corp. - FDA 510(k) Cleared Devices
1
Total
0
Cleared
1
Denied
Aibiomed, Corp. has 0 FDA 510(k) cleared medical devices. Based in Santa Barbara, US.
Active since 2018. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Aibiomed, Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Aibiomed, Corp.
1 devices