Medical Device Manufacturer · US , Redwood City , CA

Procept Biorobotics, Corporation - FDA 510(k) Cleared Devices

4 submissions · 3 cleared · Since 2017

Total

Cleared

Denied

Procept Biorobotics, Corporation has 3 FDA 510(k) cleared medical devices. Based in Redwood City, US.

Last cleared in 2023. Active since 2017. Primary specialty: Gastroenterology & Urology.

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

FDA 510(k) cleared devices by Procept Biorobotics, Corporation

4 devices

1-4 of 4