Medical Device Manufacturer · US , Woburn , MA

Cytrellis Biosystems, Inc. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2021

Total

Cleared

Denied

Cytrellis Biosystems, Inc. has 2 FDA 510(k) cleared medical devices. Based in Woburn, US.

Latest FDA clearance: Oct 2025. Active since 2021. Primary specialty: General & Plastic Surgery.

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

FDA 510(k) cleared devices by Cytrellis Biosystems, Inc.

2 devices

1-2 of 2