Allied Hill Enterprises, Ltd. is one of 20666 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Allied Hill Enterprises, Ltd. - FDA 510(k) Cleared Devices
Recent clearances: LIQUID FILLED RING TEETHER, MODEL 03807, LIQUID FILLED RING TEETHER, MODELS 1962005, 1962011, LIQUID FILLED TEETHING
1
Total
1
Cleared
0
Denied
Allied Hill Enterprises, Ltd. has 1 FDA 510(k) cleared medical devices. Based in Stoughton, US.
Historical record: 1 cleared submissions from 2009 to 2009. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Allied Hill Enterprises, Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Allied Hill Enterprises, Ltd.
1 devices