FDA 510(k) Cleared · Global Footprint · — : — : —
00 · Promaxo Platform

MRI-Guided InterventionsRight Where You See Patients.

Global presence.
Thousands of patients treated.
AI enabled imaging.

AI-assisted targeting and robotics are not yet cleared for commercial use.

01 · Position

The Point of Care MRI managing the entire patient care continuum.

The FDA 510(k) cleared Promaxo MRI platform delivers MRI-guided prostate transperineal biopsies and treatment at the clinical setting of choice. With 77% cancer detection rates versus 40% for standard-of-care TRUS biopsy1, Promaxo identifies cancer that traditional approaches miss.

From screening through biopsy to targeted treatment and follow-up, Promaxo manages the complete patient care pathway — combining point-of-care MRI, AI-assisted planning, and robotics-enabled accuracy*.

01
Screening*
02
Diagnostic Imaging
03
MRI-Guided Biopsy
04
MRI-Targeted Treatment
05
Follow-Up
02 · Practice Economics

Up to 7x higher reimbursement for biopsies and treatment compared to the standard of care.

Promaxo enables urologists to bill MRI-guided CPT codes (55713 & 55715) or (55714 & 55715) with the option to use additional MR imaging codes.

Biopsy
Up to 5x

reimbursement vs Standard of Care

Treatment
Up to 7x

reimbursement vs Standard of Care

Setting
Point-of-care

Available for clinic, ASC, or OR

04 · AI + Robotics

AI-driven screening, diagnosis, treatment, and follow-up.

Deep learning models analyze MR images for automated cancer grading. AI-powered tissue characterization enables earlier, more accurate treatment decisions. Robotics guides biopsy and treatment needles into position under live MRI.

⚠ Regulatory Clearance

Robot and AI tissue characterization are not cleared for commercial use.

AI-Driven Insights

MRI-Compatible Robot

05 · Clinical Evidence

Demonstrated clinical superiority
over standard of care.

77% cancer detection rate1. 30+ peer-reviewed publications. Global system deployment across private practices, ASCs, IDNs, and academic institutions.