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Robot maker · registered

Promaxo

Corporate marketmedicalCurated record

Promaxo integrates portable low-field MRI, AI-driven lesion localization, and robotic needle guidance into a single point-of-care platform for prostate cancer diagnosis and treatment. The MRI platform received FDA 510(k) clearance in March 2021 as the first US office-based portable MRI for prostatic lesion localization and biopsy. The system operates without facility shielding upgrades and is deployed in urology offices and outpatient surgical centres. A dedicated robotic guidance module is in development and pending separate FDA clearance.

HeadquartersOakland, US
Founded2016
Corporate funding$98M
Team51-200
Deployments3
Open roles0
01

Company overview

Identity and operating footprint

Company typeRobot maker
Market segmentCorporate
StageSeries C
FoundersAmit Vohra (CEO & President), Michael Bartholomew (Co-founder), Irving Weinberg (Co-founder)
Regions servedUS
Countries deployedNot listed
Service footprintNot listed
Last reviewed2026-07-05
MX

Robot models

Specifications remain vendor-claimed

Machinemedical

Promaxo MRI System

  • FDA 510(k) cleared for office-based MRI-guided prostate biopsy and treatment

    First US office-use portable single-sided low-field MRI system cleared for prostatic lesion localization and interventional guidance

    Claim source
DP

Deployment log

Announced and cited only

AnnouncedCustomerSiteCountryCountEvidence
2023-02-01Mount Sinai Health SystemhospitalUSNot disclosedAnnouncement
2023-02-01UTHealth HoustonhospitalUSNot disclosedAnnouncement
2021-03-08Mississippi UrologymedicalUSNot disclosedAnnouncement
CA

Funding history

Publicly announced rounds

Investors on recordZepp LabsMicroPort OrthopedicsKineticosBand of AngelsK2XZynext Ventures
TL

Company timeline

Milestones and announcements

2024-06-18Zynext Ventures (VC arm of Zydus Lifesciences) announces strategic investmentPR Newswire
2021-03-08FDA 510(k) clearance granted for office-based MRI-guided prostate biopsy systemBusinessWire
2021-03-03510(k) Premarket Notification K202518 Promaxo MRI System ↗U.S. Food and Drug Administration
SC

Source ledger

12 unique public sources