Aiex USA , Ltd. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Aiex USA , Ltd. - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Aiex USA , Ltd. has 1 FDA 510(k) cleared medical devices. Based in Rancho Cucamonga, US.
Historical record: 1 cleared submissions from 1991 to 1991. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by Aiex USA , Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Aiex USA , Ltd.
1 devices