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Francis Medical

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uuid00021cl

Namestring
Francis Medical
Legal namestring
Francis Medical, Inc.
Company typeenum
Private
Founded yearint
2018
Descriptiontext

Francis Medical, Inc. is a privately held medical device company founded in May 2018 and headquartered in Maple Grove, Minnesota, that develops convective water vapor ablation technology for the treatment of urological cancers. Its flagship product, the Vanquish Water Vapor Ablation System (commercial name Trident+), is a transurethral, ultrasound- and electromagnetically-guided device that uses the thermal (phase-shift) energy stored in sterile water vapor to convectively ablate targeted prostate tissue while preserving surrounding structures critical to urinary and sexual function. The platform originated with founder and CTO Michael Hoey, inventor of Rezum, whose prior company NxThera was acquired by Boston Scientific for up to $406M; Francis Medical has adapted the same water vapor approach from benign prostatic hyperplasia (BPH) to localized prostate cancer and is targeting bladder and kidney cancer as pipeline indications.

The company received FDA Breakthrough Device Designation in August 2023 and FDA 510(k) clearance in December 2025 for thermal ablation of targeted prostate tissue, and it is preparing a PMA submission for an expanded prostate cancer indication using 5-year VAPOR 2 follow-up data. The VAPOR 2 pivotal study completed enrollment of 235 patients across 26 U.S. sites in February 2025, with reported outcomes including 91% clearance of ≥GG2 disease at 6 months and 2.7% Grade ≥2 urinary incontinence. Francis Medical has raised approximately $157M across four funding events (Series A $18M in 2018, Coloplast $4M strategic in 2020, Series B $55M in 2021, Series C $80M in 2025) from a syndicate led by Arboretum Ventures and Solas BioVentures alongside Coloplast, Orlando Health Ventures, Tonkawa, H2Oey Ventures, and Boston Scientific.

The commercial model is a fee-per-use deployment of capital equipment (retained by Francis Medical) coupled with recurring sales of disposable Trident+ Supplies, sold directly to U.S. urology practices, ambulatory surgery centers, and hospitals under Customer Agreements. First commercial procedures began in February 2026 in Austin, Texas, and have since been executed across Arizona, Virginia, Georgia, Minnesota, San Antonio, and the Chicago metro, with international expansion targeted for 2027. Leadership comprises CEO Mike Kujak (ex-AMS, ex-NxThera), Founder/CTO Michael Hoey, and a board drawing from Fogarty Innovation, Orlando Health, and the lead venture investors.

Short descriptiontext

Francis Medical is a Maple Grove, Minnesota-based medical device company developing the Vanquish Water Vapor Ablation System, a transurethral convective water vapor platform for the treatment of localized prostate cancer in U.S. urology practices and ambulatory surgery centers on a fee-per-use model.

Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
11–50
akta.pro rankint
HeadquartersMaple Grove, United States
HQ citystring
Maple Grove
HQ countrystring
United States
HQ regionstring
North America
Markets served

Serves global market

Offices1 record

Each record includes

City, Country, Type, Description, Source

Keyword5 values
prostate cancer ablation, water vapor therapy, urology medical devices, minimally invasive thermotherapy, convective thermal ablation
Industry1 code
1Endoscopic Therapeutic & Access Devices (Trocars, dilators, biopsy/ablation tools)
CodeHLAHADANPrimaryYes
NAICS code1 code
  • Surgical and Medical Instrument Manufacturing339112
SIC code1 code
  • Surgical & Medical Instruments & Apparatus3841
Product category
Urological Medical Devices (Prostate Cancer Ablation)
GTM motion3 records

Each record includes

Type, Description, Source

Revenue model2 records
1Fee-Per-Use Capital Equipment Utilization
TypeUsage Based
Description

Customer uses the Trident+ system (capital equipment that remains owned by Francis Medical) and pays a per-use fee for each procedure under a Customer Agreement and Enrollment Form; Orders submitted via Order Form specifying the requested use dates.

francismedical.com
2Disposable Supplies (Trident+ Supplies) Sales
TypeHardware Sales
Description

Recurring purchase of disposable Trident+ Supplies required to operate the Trident+ system. Supplies must be used only with Francis Medical units and cannot be transferred to third parties. Per Occurrence rates are billed net 30; overdue balances accrue interest at 5% per month.

francismedical.com
Marketing channels7 records

Each record includes

Title, Type, Stage, Description, Source

Distribution channels2 records

Each record includes

Title, Type, Scope, Target buyer, Description, Source

Cost components6 values
Technology or R&D, Operations, Personnel, Marketing or Sales, Supply Chain, Others
Pricing details1 tier
1Fee-per-use for capital equipment + disposable Trident+ Supplies purchases
ModelUsage-basedBilling cadencePay-as-you-go
Notes

Pricing per use and supply unit prices are set in Exhibit A of the Customer Agreement and are not publicly disclosed; net-30 payment terms; 5% per month interest on overdue amounts; minimum aggregate liability cap of $1,000,000; requires commercial general liability insurance of $2,000,000 per occurrence.

francismedical.com
GTM typeB2B
B2B
Offering typeHardware or Manufacturing
Hardware or Manufacturing
Brand1 of 2 records shown
1Vanquish
Description

The Vanquish Water Vapor Ablation System — the company's flagship FDA 510(k)-cleared medical device, a transurethral, ultrasound and electromagnetically guided thermal water vapor device used to convectively ablate targeted prostate tissue via a transurethral approach.

francismedical.com
+1 more record
Core offering1 text field

Francis Medical develops, manufactures, and commercializes the Vanquish Water Vapor Ablation System (legal name: Trident+ System with Trident+ Supplies), an FDA 510(k)-cleared, transurethral, ultrasound- and electromagnetically-guided medical device that uses convective thermal energy stored in sterile water vapor to ablate targeted prostate tissue in men with localized prostate cancer. Customers (urology practices, ambulatory surgery centers, and hospitals) use the Trident+ system on a fee-per-use model under a Customer Agreement and separately purchase disposable Trident+ Supplies for each procedure, with international expansion targeted for 2027.

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 of 7 values shown
  • 91% clearance of targeted MRI-visible ≥GG2 (clinically significant) prostate disease at 6 months following a single Vanquish procedure (VAPOR 2, n=110)
+6 more records
Product overview1 text field

Francis Medical's offering is built around a single unified medical-device platform — the Vanquish Water Vapor Ablation System (also referred to under its legal product name as the Trident+ System with Trident+ Supplies) — designed as a transurethral, ultrasound- and electromagnetically-guided thermotherapy device that uses convective water vapor energy to ablate targeted prostate tissue on an outpatient basis. Supporting resources extend the offering to physicians and patients, including the eManual (electronic User Manual referenced via the site's "For Physicians" navigation), patient-facing FAQ and Physician Locator pages, and a Patient information hub (Vanquish Patient). The company also indicates a strategic direction to leverage the same underlying water vapor technology for future applications in bladder and kidney cancers, though the only commercialized product today is the Vanquish / Trident+ prostate tissue ablation system, which received FDA 510(k) clearance in late 2025 and is sold in the U.S. on a fee-per-use basis.

Product and service1 record
1Vanquish Water Vapor Ablation System (Trident+ System with Trident+ Supplies)
CategoryUrological medical device for prostate cancer ablation
Description

The Vanquish Water Vapor Ablation System (also referenced under its legal product name as the Trident+ System with disposable Trident+ Supplies) is an FDA 510(k)-cleared, transurethral, ultrasound- and electromagnetically-guided medical device that uses the thermal energy stored in sterile water vapor to convectively ablate targeted prostate tissue. The device is used on an outpatient basis under general anesthesia, enabling same-day discharge and rapid return to normal activities. It is intended for urology practices, ambulatory surgery centers, and hospitals treating men with localized prostate cancer; capital equipment is provided on a fee-per-use basis and disposable Trident+ Supplies must be purchased for each procedure.

Scale indicator7 records

Each record includes

Type, Value, Description, Source

Partnership3 partners
1The Urology Place (Dr. Naveen Kella, San Antonio, TX)
Strategic tierLead Commercial Reference SiteTypeStrategic or Co-development PartnerAnnounced on2026-05-01
Description

Dr. Naveen Kella of The Urology Place (San Antonio, TX) treated the first patient in the VAPOR 2 pivotal study in July 2023 and completed the first commercial Vanquish procedures in San Antonio at Huebner Ambulatory Surgery Center in May 2026. Functions as a key opinion leader and early commercial partner.

Strategic tierAcademic Clinical Site And Early Commercial SiteTypeStrategic or Co-development PartnerAnnounced on2026-05-01
Description

Dr. Abhinav Sidana, a urologic oncologist at University of Chicago Medicine (UChicago Medicine), served as a clinical investigator in the VAPOR 2 pivotal study and performed the first commercial Vanquish Water Vapor Ablation procedure in the Chicago metropolitan area at the Ingalls Memorial Ambulatory Surgical Center in May 2026.

Strategic tierStrategic Strategic InvestorTypeStrategic or Co-development PartnerAnnounced on2020-09-01
Description

Coloplast A/S completed a $4 million equity investment in Francis Medical in September 2020 and participated in Series B ($55M, 2021) and Series C ($80M, 2025) rounds. The investment aligns with Coloplast's Interventional Urology strategy to bring innovative solutions to the urology market. President of Coloplast Interventional Urology Steve Blum led the original announcement; Coloplast's deep urology channel and customer relationships provide strategic distribution synergies. Michele Shepard (former Coloplast, Amphora Medical executive) is VP of Clinical Affairs at Francis Medical.

Recent move14 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight7 records

Each record includes

Type, Description

Peers10 records
TypeBroad incumbent
Description

Accuray's CyberKnife stereotactic body radiation therapy (SBRT) is a non-invasive treatment alternative for localized prostate cancer. It competes with Vanquish in the broader localized prostate cancer treatment landscape, particularly for patients seeking organ-preserving options.

TypeEmerging player
Description

Koelis provides MRI-ultrasound fusion biopsy and prostate imaging/guidance technology used alongside focal-therapy procedures. It is an emerging adjacent player whose products intersect with Vanquish-enabled workflows in urology practices performing targeted prostate ablation.

TypeDirect peer
Description

Galil Medical (acquired by Penumbra) provides cryoablation systems used for prostate tissue ablation as a focal-therapy alternative. It competes with Vanquish for urology oncology share with a longer commercial track record and established reimbursement.

TypeDirect peer
Description

EDAP TMS markets the Focal One robotic HIFU platform for prostate tissue ablation, the most direct focal-therapy competitor to Francis Medical's Vanquish. Both target urologists treating localized prostate cancer with minimally invasive, organ-preserving approaches.

TypeDirect peer
Description

Profound Medical's TULSA-PRO system uses MRI-guided transurethral ultrasound ablation of prostate tissue. Like Vanquish, it is a transurethral, minimally invasive, outpatient prostate ablation technology directly competing for urology practice adoption and focal-therapy share.

TypeBroad incumbent
Description

Boston Scientific acquired NxThera's Rezum water vapor technology for BPH and is also a co-investor in Francis Medical's Series A. As the established owner of the original water vapor platform in urology, it is a broad incumbent with overlapping urology commercial channels and a related technology base.

TypeBroad incumbent
Description

Varian, now part of Siemens Healthineers, provides radiation therapy (including brachytherapy and external beam) that competes against Vanquish as a non-surgical treatment for localized prostate cancer. It is a broad incumbent with deep oncology infrastructure and established reimbursement.

TypeDirect peer
Description

HealthTronics offers cryoablation and other minimally invasive urology procedures for prostate cancer treatment. It is a direct peer competing in the focal-therapy / prostate ablation space with established physician relationships and service-based delivery models.

TypeDirect peer
Description

AngioDynamics markets the NanoKnife irreversible electroporation (IRE) system, which is used for prostate tissue ablation as a focal-therapy alternative. It targets similar urology oncology customers and competes in the same minimally invasive prostate cancer treatment category as Vanquish.

TypeDirect peer
Description

SonaCare Medical's Sonablate HIFU system is a transrectal high-intensity focused ultrasound device for prostate tissue ablation. It is a direct focal-therapy alternative to Vanquish, competing for the same urology accounts and intermediate-risk prostate cancer patient population.

Market position
Strengths5 records

Each record includes

Headline, Details, Source

Weaknesses5 records

Each record includes

Headline, Details, Source

Competitive moat6 records

Each record includes

Type, Details

Key risks6 records

Each record includes

Headline, Details, Source

Key highlights7 records

Each record includes

Headline, Details, Source

Customer concentration

Classification, Details

Named customers7 records

Each record includes

Name, Industry, Type, Use case, Source, UUID

Segment4 records

Each record includes

Title, Type, Primary, Description, Pain point addressed, Use case, Source

Ideal customer profile2 records

Each record includes

Profile, Firmographic size, Sales motion, Sales cycle length, Buying structure, Purchase trigger, Buyer persona, Geography, Industry vertical, Primary use case, Description, Pain points, Evidence proof points, Target buyer

Technology focused
Yes
API detail
Has APIbool
No

Docs URL, Description

AI maturity
App detail

Has app

Feature5 records

Each record includes

Title, Differentiator, Description, Source

Core technology
Revenue estimate
Valuation estimate
Number of profiles
Profiles15 records

Each record includes

Name, Designation, Designation category, Overview, Profile commentary, Source

Subsidiaries1 record

Each record includes

Name, Acquired on, Relationship type, Type, Business focus

Compliance2 records

Each record includes

Name, Class, Description

Funding overview

Funding stage, Last funding date, Total funding USD

Funding rounds4 records

Each record includes

Round, Amount USD, Date, Pre money valuation, Total investors, Investors, News

Investors6 records

Each record includes

Name, Type, Date of entry, Rounds participated, Website

Funding detail is available on the Subscription and Enterprise plan.Contact sales →

M&A

Each record includes

Name, Acquisition type, Announced date, Completed date, Status, Website, News

Investment

Each record includes

Name, Round, Announced date, Lead investor, Website, News

M&A and investment is available on the Subscription and Enterprise plan.Contact sales →

Francis Medical

Urological Medical Devices (Prostate Cancer Ablation)francismedical.com

Francis Medical is a Maple Grove, Minnesota-based medical device company developing the Vanquish Water Vapor Ablation System, a transurethral convective water vapor platform for the treatment of localized prostate cancer in U.S. urology practices and ambulatory surgery centers on a fee-per-use model.

What Francis Medical does

Francis Medical, Inc. is a privately held medical device company founded in May 2018 and headquartered in Maple Grove, Minnesota, that develops convective water vapor ablation technology for the treatment of urological cancers. Its flagship product, the Vanquish Water Vapor Ablation System (commercial name Trident+), is a transurethral, ultrasound- and electromagnetically-guided device that uses the thermal (phase-shift) energy stored in sterile water vapor to convectively ablate targeted prostate tissue while preserving surrounding structures critical to urinary and sexual function. The platform originated with founder and CTO Michael Hoey, inventor of Rezum, whose prior company NxThera was acquired by Boston Scientific for up to $406M; Francis Medical has adapted the same water vapor approach from benign prostatic hyperplasia (BPH) to localized prostate cancer and is targeting bladder and kidney cancer as pipeline indications.

The company received FDA Breakthrough Device Designation in August 2023 and FDA 510(k) clearance in December 2025 for thermal ablation of targeted prostate tissue, and it is preparing a PMA submission for an expanded prostate cancer indication using 5-year VAPOR 2 follow-up data. The VAPOR 2 pivotal study completed enrollment of 235 patients across 26 U.S. sites in February 2025, with reported outcomes including 91% clearance of ≥GG2 disease at 6 months and 2.7% Grade ≥2 urinary incontinence. Francis Medical has raised approximately $157M across four funding events (Series A $18M in 2018, Coloplast $4M strategic in 2020, Series B $55M in 2021, Series C $80M in 2025) from a syndicate led by Arboretum Ventures and Solas BioVentures alongside Coloplast, Orlando Health Ventures, Tonkawa, H2Oey Ventures, and Boston Scientific.

The commercial model is a fee-per-use deployment of capital equipment (retained by Francis Medical) coupled with recurring sales of disposable Trident+ Supplies, sold directly to U.S. urology practices, ambulatory surgery centers, and hospitals under Customer Agreements. First commercial procedures began in February 2026 in Austin, Texas, and have since been executed across Arizona, Virginia, Georgia, Minnesota, San Antonio, and the Chicago metro, with international expansion targeted for 2027. Leadership comprises CEO Mike Kujak (ex-AMS, ex-NxThera), Founder/CTO Michael Hoey, and a board drawing from Fogarty Innovation, Orlando Health, and the lead venture investors.

Francis Medical firmographics

Firmographics
Name
Francis Medical
Legal name
Francis Medical, Inc.
Website
https://francismedical.com
Company type
Private
Founded year
2018
Operating status
Operating
Headcount range
11–50 employees
Short description
Francis Medical is a Maple Grove, Minnesota-based medical device company developing the Vanquish Water Vapor Ablation System, a transurethral convective water vapor platform for the treatment of localized prostate cancer in U.S. urology practices and ambulatory surgery centers on a fee-per-use model.
Ownership category
akta.pro rank

Francis Medical industry classification

Industry
Product category
Urological Medical Devices (Prostate Cancer Ablation)
NAICS
Surgical and Medical Instrument Manufacturing (339112)
SIC
Surgical & Medical Instruments & Apparatus (3841)
akta.pro primary industry
Endoscopic Therapeutic & Access Devices (Trocars, dilators, biopsy/ablation tools) (HLAHADAN)

Keywords

  • Prostate cancer ablation
  • Water vapor therapy
  • Urology medical devices
  • Minimally invasive thermotherapy
  • Convective thermal ablation

Where Francis Medical is headquartered

Location

Headquarters

HQ city
Maple Grove
HQ country
United States
HQ region
North America

Offices1 record

Markets served

Francis Medical business model

Business model
GTM type
B2B
Offering type
Hardware or Manufacturing
Cost components
Technology or R&D, Operations, Personnel, Marketing or Sales, Supply Chain, Others

Revenue model

  1. Fee-Per-Use Capital Equipment Utilization: Customer uses the Trident+ system (capital equipment that remains owned by Francis Medical) and pays a per-use fee for each procedure under a Customer Agreement and Enrollment Form; Orders submitted via Order Form specifying the requested use dates.
  2. Disposable Supplies (Trident+ Supplies) Sales: Recurring purchase of disposable Trident+ Supplies required to operate the Trident+ system. Supplies must be used only with Francis Medical units and cannot be transferred to third parties. Per Occurrence rates are billed net 30; overdue balances accrue interest at 5% per month.

Pricing tiers

ModelBillingPrice
Usage-basedPay-as-you-goFee-per-use for capital equipment + disposable Trident+ Supplies purchases

Go-to-market motion3 records

Distribution channels2 records

Marketing channels7 records

Francis Medical product offering

Product offering

Core offering

Francis Medical develops, manufactures, and commercializes the Vanquish Water Vapor Ablation System (legal name: Trident+ System with Trident+ Supplies), an FDA 510(k)-cleared, transurethral, ultrasound- and electromagnetically-guided medical device that uses convective thermal energy stored in sterile water vapor to ablate targeted prostate tissue in men with localized prostate cancer. Customers (urology practices, ambulatory surgery centers, and hospitals) use the Trident+ system on a fee-per-use model under a Customer Agreement and separately purchase disposable Trident+ Supplies for each procedure, with international expansion targeted for 2027.

Product overview

Francis Medical's offering is built around a single unified medical-device platform — the Vanquish Water Vapor Ablation System (also referred to under its legal product name as the Trident+ System with Trident+ Supplies) — designed as a transurethral, ultrasound- and electromagnetically-guided thermotherapy device that uses convective water vapor energy to ablate targeted prostate tissue on an outpatient basis. Supporting resources extend the offering to physicians and patients, including the eManual (electronic User Manual referenced via the site's "For Physicians" navigation), patient-facing FAQ and Physician Locator pages, and a Patient information hub (Vanquish Patient). The company also indicates a strategic direction to leverage the same underlying water vapor technology for future applications in bladder and kidney cancers, though the only commercialized product today is the Vanquish / Trident+ prostate tissue ablation system, which received FDA 510(k) clearance in late 2025 and is sold in the U.S. on a fee-per-use basis.

Differentiator

Problem solved

Functional benefit

Brands

  • Vanquish: The Vanquish Water Vapor Ablation System — the company's flagship FDA 510(k)-cleared medical device, a transurethral, ultrasound and electromagnetically guided thermal water vapor device used to convectively ablate targeted prostate tissue via a transurethral approach.
  • Trident+ System

Products and services

  • Vanquish Water Vapor Ablation System (Trident+ System with Trident+ Supplies) The Vanquish Water Vapor Ablation System (also referenced under its legal product name as the Trident+ System with disposable Trident+ Supplies) is an FDA 510(k)-cleared, transurethral, ultrasound- and electromagnetically-guided medical device that uses the thermal energy stored in sterile water vapor to convectively ablate targeted prostate tissue. The device is used on an outpatient basis under general anesthesia, enabling same-day discharge and rapid return to normal activities. It is intended for urology practices, ambulatory surgery centers, and hospitals treating men with localized prostate cancer; capital equipment is provided on a fee-per-use basis and disposable Trident+ Supplies must be purchased for each procedure.

Quantifiable outcome

  • 91% clearance of targeted MRI-visible ≥GG2 (clinically significant) prostate disease at 6 months following a single Vanquish procedure (VAPOR 2, n=110)
  • +6 more outcomes

Companies that use Francis Medical

Customer profile

Named customers7 records

Segments4 records

Ideal customer profiles2 records

Francis Medical technology and API

Technology

Technology focussed Yes

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

Feature5 records

Francis Medical partnerships and signals

Strategic signal

Partnerships

Three partnerships are on record, tiered lead commercial reference site, academic clinical site and early commercial site and strategic strategic investor.

  • The Urology Place (Dr. Naveen Kella, San Antonio, TX)lead commercial reference siteStrategic or Co-development Partner · 1 May 2026Dr. Naveen Kella of The Urology Place (San Antonio, TX) treated the first patient in the VAPOR 2 pivotal study in July 2023 and completed the first commercial Vanquish procedures in San Antonio at Huebner Ambulatory Surgery Center in May 2026. Functions as a key opinion leader and early commercial partner.
  • University of Chicago Medicine (Dr. Abhinav Sidana)academic clinical site and early commercial siteStrategic or Co-development Partner · 1 May 2026Dr. Abhinav Sidana, a urologic oncologist at University of Chicago Medicine (UChicago Medicine), served as a clinical investigator in the VAPOR 2 pivotal study and performed the first commercial Vanquish Water Vapor Ablation procedure in the Chicago metropolitan area at the Ingalls Memorial Ambulatory Surgical Center in May 2026.
  • Coloplast A/Sstrategic strategic investorStrategic or Co-development Partner · 1 September 2020Coloplast A/S completed a $4 million equity investment in Francis Medical in September 2020 and participated in Series B ($55M, 2021) and Series C ($80M, 2025) rounds. The investment aligns with Coloplast's Interventional Urology strategy to bring innovative solutions to the urology market. President of Coloplast Interventional Urology Steve Blum led the original announcement; Coloplast's deep urology channel and customer relationships provide strategic distribution synergies. Michele Shepard (former Coloplast, Amphora Medical executive) is VP of Clinical Affairs at Francis Medical.

Scale indicators7 records

Recent moves14 records

Expansion highlights7 records

Francis Medical competitors and assessment

Company assessment

Broad incumbents

  • Accuray: Accuray's CyberKnife stereotactic body radiation therapy (SBRT) is a non-invasive treatment alternative for localized prostate cancer. It competes with Vanquish in the broader localized prostate cancer treatment landscape, particularly for patients seeking organ-preserving options.
  • Boston Scientific: Boston Scientific acquired NxThera's Rezum water vapor technology for BPH and is also a co-investor in Francis Medical's Series A. As the established owner of the original water vapor platform in urology, it is a broad incumbent with overlapping urology commercial channels and a related technology base.
  • Varian (Siemens Healthineers): Varian, now part of Siemens Healthineers, provides radiation therapy (including brachytherapy and external beam) that competes against Vanquish as a non-surgical treatment for localized prostate cancer. It is a broad incumbent with deep oncology infrastructure and established reimbursement.

Emerging players

  • Koelis: Koelis provides MRI-ultrasound fusion biopsy and prostate imaging/guidance technology used alongside focal-therapy procedures. It is an emerging adjacent player whose products intersect with Vanquish-enabled workflows in urology practices performing targeted prostate ablation.

Direct peers

  • Galil Medical (Penumbra): Galil Medical (acquired by Penumbra) provides cryoablation systems used for prostate tissue ablation as a focal-therapy alternative. It competes with Vanquish for urology oncology share with a longer commercial track record and established reimbursement.
  • EDAP TMS: EDAP TMS markets the Focal One robotic HIFU platform for prostate tissue ablation, the most direct focal-therapy competitor to Francis Medical's Vanquish. Both target urologists treating localized prostate cancer with minimally invasive, organ-preserving approaches.
  • Profound Medical: Profound Medical's TULSA-PRO system uses MRI-guided transurethral ultrasound ablation of prostate tissue. Like Vanquish, it is a transurethral, minimally invasive, outpatient prostate ablation technology directly competing for urology practice adoption and focal-therapy share.
  • HealthTronics: HealthTronics offers cryoablation and other minimally invasive urology procedures for prostate cancer treatment. It is a direct peer competing in the focal-therapy / prostate ablation space with established physician relationships and service-based delivery models.
  • AngioDynamics: AngioDynamics markets the NanoKnife irreversible electroporation (IRE) system, which is used for prostate tissue ablation as a focal-therapy alternative. It targets similar urology oncology customers and competes in the same minimally invasive prostate cancer treatment category as Vanquish.
  • Sonablate / SonaCare Medical: SonaCare Medical's Sonablate HIFU system is a transrectal high-intensity focused ultrasound device for prostate tissue ablation. It is a direct focal-therapy alternative to Vanquish, competing for the same urology accounts and intermediate-risk prostate cancer patient population.

Market position

Strengths5 records

Weaknesses5 records

Competitive moat6 records

Key risks6 records

Key highlights7 records

Customer concentration

Francis Medical social profiles

Digital presence

Francis Medical compliance and trust

Trust signal

Compliance2 records

Francis Medical financial estimates

Financial estimate

Revenue estimate

Valuation estimate

Francis Medical leadership team

Management profile

Number of profiles

Profiles15 records

Francis Medical subsidiaries and ownership

Company hierarchy

Subsidiaries1 record

Francis Medical funding detail

Funding detail

Funding overview

Funding rounds4 records

Investors6 records

Funding detail is available on the Subscription and Enterprise plan.Contact sales →

Francis Medical M&A and investment

M&A and investment

M&A

Investments

M&A and investment is available on the Subscription and Enterprise plan.Contact sales →

Frequently asked questions about Francis Medical

What does Francis Medical do?

Francis Medical develops, manufactures, and commercializes the Vanquish Water Vapor Ablation System (legal name: Trident+ System with Trident+ Supplies), an FDA 510(k)-cleared, transurethral, ultrasound- and electromagnetically-guided medical device that uses convective thermal energy stored in sterile water vapor to ablate targeted prostate tissue in men with localized prostate cancer. Customers (urology practices, ambulatory surgery centers, and hospitals) use the Trident+ system on a fee-per-use model under a Customer Agreement and separately purchase disposable Trident+ Supplies for each procedure, with international expansion targeted for 2027.

Is Francis Medical a public or private company?

Francis Medical is a private company. It is classified as venture growth investor backed and is currently operating.

When was Francis Medical founded?

Francis Medical was founded in 2018. It employs 11 to 50 people.

Where is Francis Medical based?

Francis Medical is headquartered in Maple Grove, United States, in the North America region.

How does Francis Medical make money?

Two revenue lines are on record. Fee-Per-Use Capital Equipment Utilization is the primary driver. The others are disposable Supplies (Trident+ Supplies) Sales.

Who are Francis Medical's main competitors?

Broad incumbents on record are Accuray, Boston Scientific and Varian (Siemens Healthineers). Koelis is listed as an emerging player. Direct peers are Galil Medical (Penumbra), EDAP TMS, Profound Medical, HealthTronics, AngioDynamics and Sonablate / SonaCare Medical.

Does Francis Medical have an API?

No public API is recorded for Francis Medical.

What industry is Francis Medical in?

Francis Medical's product category is Urological Medical Devices (Prostate Cancer Ablation). Its primary akta.pro industry code is HLAHADAN, Endoscopic Therapeutic & Access Devices (Trocars, dilators, biopsy/ablation tools). Its NAICS code is 339112 and its SIC code is 3841.

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Live signals
PR NewswireFrancis Medical Announces Northwell Urology Group Performs First Commercial Vanquish® Water Vapor Ablation Procedure in New YorkSamir S. Taneja, MD, performed the first commercial Vanquish Water Vapor Ablation procedure in New York at Northwell Health in Lake Success. The procedure was on an outpatient basis for a patient with localized prostate cancer. The VAPOR 2 study showed 91% elimination of targeted disease after one procedure.PR NewswireFrancis Medical Announces Orange County Urology Associates Becomes First in California to Integrate Vanquish® Water Vapor Ablation into Routine Prostate CareDr. Daniel Su at Orange County Urology Associates performed California's first commercial Vanquish Water Vapor Ablation procedures, a minimally invasive FDA-cleared technology developed by Francis Medical for targeted prostate tissue treatment. The VAPOR 2 clinical trial demonstrated 91% elimination of targeted MRI-visible intermediate-risk disease at six months with no device-related serious adverse events, and 93% patient satisfaction at 12 months. Francis Medical CEO Mike Kujak stated the early adoption validates the technology's practicality for real-world urology practice deployment.BioSpaceFrancis Medical Announces Publication of VAPOR 2 Pivotal Trial Results in The Journal of UrologyFrancis Medical published initial VAPOR 2 trial results in The Journal of Urology, reporting 91% clearance of targeted prostate cancer lesions after a single treatment and 93% patient satisfaction. The multicenter study enrolled 110 patients, with no device-related serious adverse events. The trial will follow patients for five years to support a pre-market approval submission.PR NewswireFrancis Medical Announces Publication of VAPOR 2 Pivotal Trial Results in The Journal of UrologyFrancis Medical announced the publication of initial results from its VAPOR 2 pivotal clinical trial in The Journal of Urology, evaluating the Vanquish Water Vapor Ablation System in 110 patients with intermediate-risk, localized prostate cancer across 26 U.S. clinical sites. Key findings included 91% clearance of targeted disease after a single treatment, no device-related serious adverse events, low rates of urinary incontinence and erectile dysfunction, and 93% patient satisfaction. The company stated the study will continue following patients to five years to support a pre-market approval submission to the FDA.PR NewswireUniversity of Chicago Urologist Performs First Commercial Vanquish® Water Vapor Ablation Procedures in the StateDr. Abhinav Sidana, a urologic oncologist at University of Chicago Medicine, performed the first commercial Vanquish® Water Vapor Ablation procedure in the Chicago metropolitan area on a patient with localized prostate cancer. The Vanquish System, developed by Minnesota-based Francis Medical, received FDA 510(k) clearance in late 2025 and uses thermal energy stored in sterile water vapor to ablate targeted prostate tissue through a transurethral approach. This milestone marks the first commercial use of the technology outside of a clinical study, making a minimally invasive prostate treatment option newly available to patients in the Illinois region.PR NewswireFrancis Medical Announces Further Expansion of Commercial Vanquish® Procedures to Ablate Prostate TissueFrancis Medical announced the first commercial Vanquish Water Vapor Ablation procedures in San Antonio, Texas, performed by Dr. Naveen Kella. The VAPOR 2 study showed 91% negative biopsy at six months and 93% patient satisfaction. The study continues to five years to support a pre-market approval submission.openPR.comSegmentation, Major Trends, and Competitive Overview of the Oncology Companion Diagnostics MarketThe oncology companion diagnostics market is projected to grow from its current size to $6.5 billion by 2030, representing a compound annual growth rate of 10.9%, driven by advancements in next-generation sequencing, PCR-based diagnostics, and increased adoption of precision oncology treatments. In early 2024, Agilent Technologies Inc. partnered with Incyte Corporation to expand Agilent's companion diagnostics portfolio and support Incyte's oncology and hematology therapies. Additionally, in August 2023, Francis Medical Inc. received Breakthrough Device Designation from the U.S. FDA for its Vanquish water vapor ablation therapy system designed to treat prostate cancer.PR NewswireFrancis Medical Announces First Commercial Vanquish® Procedure to Ablate Prostate Tissue in the MidwestFrancis Medical announced the successful completion of the first commercial Vanquish Water Vapor Ablation System procedure in the Midwest by Dr. Aaron Milbank of Minnesota Urology at High Pointe Surgery Center in Lake Elmo, Minnesota, on a patient with localized prostate cancer. The procedure marks the transition from the VAPOR 2 pivotal clinical study to real-world commercial adoption, supported by clinical data showing 91% of eligible patients achieved clearance of clinically significant in-field disease with no device-related serious adverse events. The company plans to continue patient follow-up to gather longer-term outcomes supporting a pre-market approval submission for an expanded prostate cancer indication.PR NewswireFrancis Medical Announces Further Commercial Expansion of Vanquish® Water Vapor Ablation with First Commercial Procedures to Ablate Targeted Prostate Tissue in the SoutheastFrancis Medical announced the expansion of its U.S. commercial launch for the Vanquish Water Vapor Ablation System to the Southeast, with first procedures performed at Advanced Urology centers in Atlanta by urologists Neal Patel and Jason Lomboy. The FDA-cleared system, which received approval in November 2025, uses high-energy sterile water vapor to ablate targeted prostate tissue in a minimally invasive procedure. Clinical data from the ongoing VAPOR 2 pivotal study shows 91% of patients achieved clearance of clinically significant in-field disease at six months with no device-related serious adverse events.PR NewswireFrancis Medical Announces First Commercial Vanquish® Procedure on the East Coast for Prostate Tissue AblationFrancis Medical, Inc. announced the successful completion of the first commercial Vanquish Water Vapor Ablation System procedure on the East Coast, performed by Dr. Robert Given at Chesapeake Regional Surgery Center in Virginia Beach on a patient with localized prostate cancer. The Vanquish System, which received FDA 510(k) clearance in November 2025, showed in its VAPOR 2 pivotal study that 91% of eligible patients had negative biopsy at six months with no device-related serious adverse events and high patient satisfaction rates. The company plans to continue patient follow-up to support a pre-market approval submission for an expanded indication treating clinically localized prostate cancer.