AIOBIO Co., Ltd. is one of 351 FDA 510(k) medical device manufacturers from South Korea in the dataset, ranked by real submission volume.
AIOBIO Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Qraycam PRO, Qraypen
2
Total
2
Cleared
0
Denied
AIOBIO Co., Ltd. has 2 FDA 510(k) cleared medical devices. Based in Seongnam-Si, KR.
Latest FDA clearance: Sep 2024. Active since 2019. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by AIOBIO Co., Ltd. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Mdlab and KMC, Inc..
FDA 510(k) Regulatory Record - AIOBIO Co., Ltd.
2 devices