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AquaBeam Handpiece

PROCEPT BioRobotics Corporation · Model HP2000 · UDI-DI 00850055427037

PZP
1
510(k) clearances
1,449
Adverse events (35 deaths)
2
Recalls
9
Facilities

Recalls

DateFirmReason
2021-07-09PROCEPT BIOROBOTICS CORPORATIONScope tube tip may detach from the telescoping tube, which is attached to a single-use handpiece, a component of an aquablation robotic system. Both tip detachment and entire tip s
2019-03-06PROCEPT BIOROBOTICS CORPORATIONCertain lots may develop an internal leak due to a micro-crack in a specific weld joint within the device. When the Robot detects this failure, it immediately renders the device in

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.