Faceheart Corp. - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Faceheart Corp. has 2 FDA 510(k) cleared medical devices. Based in Grand Cayman, KY.
Latest FDA clearance: Apr 2025. Active since 2023. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Faceheart Corp. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Facehart Corp. as regulatory consultant.
2 devices