Fesariustherapeutics, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Fesariustherapeutics, Inc. - FDA 510(k) Cleared Devices
Recent clearances: DermiSphere Dermal Template
1
Total
1
Cleared
0
Denied
Fesariustherapeutics, Inc. has 1 FDA 510(k) cleared medical devices. Based in Brooklyn, US.
Latest FDA clearance: Jan 2025. Active since 2025. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Fesariustherapeutics, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Regenity Biosciences as regulatory consultant.
FDA 510(k) Regulatory Record - Fesariustherapeutics, Inc.
1 devices