Shenzhen Aeon Technology Co., Ltd. is one of 1554 FDA 510(k) medical device manufacturers from China in the dataset, ranked by real submission volume.
Shenzhen Aeon Technology Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Pulse Oximeter, Pulse Oximeter
3
Total
3
Cleared
0
Denied
Shenzhen Aeon Technology Co., Ltd. has 3 FDA 510(k) cleared medical devices. Based in Shenzhen, CN.
Historical record: 3 cleared submissions from 2017 to 2020. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Shenzhen Aeon Technology Co., Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Chonconn Medical Device Consulting Co., Ltd. as regulatory consultant.
FDA 510(k) Regulatory Record - Shenzhen Aeon Technology Co., Ltd.
3 devices