Allen J. Moses, Dds, Ltd. is one of 18413 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Allen J. Moses, Dds, Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Apinator, The Moses Express appliance, THE MOSES ELITE APPLIANCE
4
Total
4
Cleared
0
Denied
Allen J. Moses, Dds, Ltd. has 4 FDA 510(k) cleared medical devices. Based in Chicago, US.
Historical record: 4 cleared submissions from 2010 to 2016. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Allen J. Moses, Dds, Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Gloria Pacini as regulatory consultant.
FDA 510(k) Regulatory Record - Allen J. Moses, Dds, Ltd.
4 devices