Procept Biorobotics, Corporation FDA Approvals

0 new drug approvals and 3 device clearances on file. This applicant is not matched to a listed company.

Newest first

A new drug approval is an original application; a 510(k) is a device shown equivalent to one already sold.

Product	What it is	Route	Decided
AquaBeam Robotic System510(k)Aug 30, 2023General, Plastic Surgery	General, Plastic Surgery	510(k)Substantially Equivalent (Traditional)	Aug 30, 2023
AquaBeam Robotic System510(k)Oct 6, 2021General, Plastic Surgery	General, Plastic Surgery	510(k)Substantially Equivalent (Special)	Oct 6, 2021
AquaBeam Robotic System510(k)Mar 11, 2021General, Plastic Surgery	General, Plastic Surgery	510(k)Substantially Equivalent (Traditional)	Mar 11, 2021