Forest Devices, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Forest Devices, Inc. - FDA 510(k) Cleared Devices
Recent clearances: SignalNED System (Model RE), SignalNED System (Model RE)
2
Total
2
Cleared
0
Denied
Forest Devices, Inc. has 2 FDA 510(k) cleared medical devices. Based in Pittsburgh, US.
Latest FDA clearance: Sep 2025. Active since 2024. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Forest Devices, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Third Party Review Group, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Forest Devices, Inc.
2 devices