T.A. Coleman Ent. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
T.A. Coleman Ent. - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
T.A. Coleman Ent. has 1 FDA 510(k) cleared medical devices. Based in Washington, US.
Historical record: 1 cleared submissions from 1998 to 1998. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by T.A. Coleman Ent. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - T.A. Coleman Ent.
1 devices