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ClearPoint Maestro

Clearpoint Neuro, Inc. · Model CPM-SFW-1 · UDI-DI 00850359007966

QIH Prescription
10
510(k) clearances
10
Adverse events
2
Recalls
236
Facilities

Description

ClearPoint Maestro Brain Model Software Version 1.0

Recalls

DateFirmReason
2026-05-07PIE Medical Imaging B.V.User measurement value reported by diagnostic bioimaging software intended to measure/visualize cardiovascular structures may be larger (0.8% to 34.4%) than the actual anatomical d
2021-05-19Caption HealthThe firm is aware of a issue with ultrasound software that results in unintended video frames being included. This could lead to an incorrect automated ejection fraction (AutoE

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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.