Forest Devices, Inc. - FDA 510(k) Cleared Devices
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.
2 devices