Medical Device Manufacturer · US , Brooklyn , NY

Cresilon, Inc. - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 2023

Total

Cleared

Denied

Cresilon, Inc. has 3 FDA 510(k) cleared medical devices. Based in Brooklyn, US.

Latest FDA clearance: Dec 2025. Active since 2023. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by Cresilon, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) cleared devices by Cresilon, Inc.

3 devices

1-3 of 3