AIOBIO Co., Ltd. - FDA 510(k) Cleared Devices
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.
510(k) submissions have been managed by KMC, Inc. as regulatory consultant.
2 devices