Pain Management Technologies, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Pain Management Technologies, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Armory Motion
1
Total
1
Cleared
0
Denied
Pain Management Technologies, Inc. has 1 FDA 510(k) cleared medical devices. Based in Akron, US.
Last cleared in 2022. Active since 2022. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Pain Management Technologies, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Pain Management Technologies, Inc.
1 devices