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DeepQure

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uuid000acql

Namestring
DeepQure
Legal namestring
DeepQure Inc.
Company typeenum
Private
Founded yearint
2019
Descriptiontext

DeepQure Inc. is a Seoul, South Korea-based clinical-stage medical device company developing HyperQure, the world's first laparoscopic extravascular renal denervation (RDN) system for the treatment of resistant hypertension. The company's core technology delivers temperature-controlled radiofrequency (RF) energy from outside the renal artery using a segmented electrode tip that wraps circumferentially around the vessel, enabling complete 360-degree denervation regardless of nerve distribution. Three electrode sizes address renal arteries ranging from 2mm to 11mm in diameter, covering branched and accessory arteries that catheter-based intravascular RDN systems cannot reach. The system is compatible with both laparoscopic and robotic (da Vinci SP single-port) surgical platforms and comprises a generator base unit, a shaft and electrode assembly, and a surgeon-controlled handle with safety features including an emergency release system.

The company originated from government-funded research initiated by co-founder Dr. Chang-Wook Jeong at Seoul National University Hospital and was incorporated as DeepQure Inc. DeepQure is currently conducting first-in-human trials in Korea (10 patients enrolled, completed December 2025) and an Early Feasibility Study across six leading US academic medical centers (Stanford, Mayo Clinic, Emory, UC Irvine, University of Florida, Henry Ford Health), with IRB approvals secured. The company has filed 170+ patents across more than 10 countries, received MFDS Breakthrough Device Designation (Innovative Medical Device No. 36, July 2023), and FDA Investigational Device Exemption approval (June 2024). The pipeline extends beyond hypertension to atrial fibrillation (MFDS cleared July 2025) and other sympathetic-mediated cardiovascular indications.

DeepQure's business model is anchored on direct enterprise sales of the HyperQure Class III medical device to hospital systems following FDA Pre-Market Approval and Korean MFDS clearance, with pricing benchmarked against industry RDN procedural costs of US$5,000-$10,000 per procedure. The company is also pursuing strategic collaboration with global medtech partners for potential co-development or market development. To date, DeepQure has raised approximately $18 million in total venture funding, most recently via a Series C round (April 2025) led by Sui Generis Partners (수이제네리스 파트너스). The company operates with a leadership team combining clinical innovators (CMO Dr. Jeong), finance executives (Chairman Chan-Ho Park, ex-Goldman Sachs/Warburg Pincus), and regulatory specialists (Global VP Jason G. Jones, ex-SoniVie), and has not yet generated commercial revenue.

Short descriptiontext

DeepQure is a clinical-stage Korean medical device company developing HyperQure, the world's first laparoscopic extravascular renal denervation system for treating resistant hypertension, with an expanding pipeline into atrial fibrillation.

Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
1–10
akta.pro rankint
HeadquartersSeoul, South Korea
HQ citystring
Seoul
HQ countrystring
South Korea
HQ regionstring
Asia
Markets served

Serves global market

Offices1 record

Each record includes

City, Country, Type, Description, Source

Keyword5 values
renal denervation devices, extravascular RDN system, resistant hypertension treatment, laparoscopic medical devices, radiofrequency ablation
Industry1 code
1HLAHAKAI
CodeHLAHAKAIPrimaryYes
NAICS code2 codes
  • 339112
  • 621492
SIC code2 codes
  • 3841
  • 7372
Product category
Renal Denervation Medical Devices
Social media profiles1 record
GTM motion1 record

Each record includes

Type, Description, Source

Revenue model1 record
1Medical Device Hardware Sales
TypeHardware Sales
Description

DeepQure is a clinical-stage medtech company developing and preparing to commercialize the HyperQure extravascular RDN system. As a Class III medical device targeting hospital-based interventional procedures, revenue will be generated through direct device sales to hospital systems following regulatory approval (FDA PMA / Korean MFDS). The company is also exploring strategic partnerships with global medtech firms.

deepqure.com
Marketing channels6 records

Each record includes

Title, Type, Stage, Description, Source

Distribution channels1 record

Each record includes

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

Cost components4 values
Technology or R&D, Personnel, Operations, Marketing or Sales
GTM typeB2B
B2B
Offering typeHardware or Manufacturing
Hardware or Manufacturing
Brand1 record
1HyperQure
Description

The world's first laparoscopic extravascular renal denervation (RDN) system designed for 360° circumferential ablation of renal nerves from outside the vessel. HyperQure is a next-generation RDN device targeting resistant hypertension and atrial fibrillation.

deepqure.com
Core offering1 text field

DeepQure is developing and preparing to commercialize the HyperQure system, the world's first laparoscopic extravascular renal denervation (RDN) device. It performs 360-degree circumferential RF ablation of renal nerves from outside the renal artery for treating resistant hypertension. The system consists of a Generator (RF energy source), Shaft and Electrode (surgical instrument with three electrode sizes for 2-11mm arteries), and Handle (surgeon control with safety features), and is compatible with laparoscopic and single-port robotic surgery.

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 of 8 values shown
  • 51 mmHg average reduction in systolic blood pressure at 12 months in Korean first-in-human study (baseline 165 mmHg to 114 mmHg)
+7 more records
Product overview1 text field

DeepQure offers HyperQure, the world's first laparoscopic extravascular renal denervation (RDN) system. The core HyperQure RDN System consists of three integrated components: a Generator (RF energy source), Shaft and Electrode (surgical instrument), and Handle (surgeon control interface). The system performs 360° circumferential nerve ablation from outside the renal artery using temperature-controlled RF ablation. A variant, HyperQure RDM System, is being developed for atrial fibrillation treatment. All products are currently in clinical trial stage.

Product and service2 records
1HyperQure RDN System
CategoryRenal Denervation Medical Device
Description

World's first laparoscopic extravascular renal denervation system that delivers radiofrequency energy from outside the renal artery for complete 360-degree circumferential nerve ablation. Consists of Generator (RF energy source and control unit), Shaft and Electrode (surgical instrument that wraps around the renal artery to deliver RF energy), and Handle (surgeon control interface with safety features). Designed for treating resistant hypertension in hospital-based interventional settings, with three electrode sizes covering renal arteries from 2mm to 11mm in diameter.

2HyperQure RDM System
CategoryRenal Denervation Medical Device - Atrial Fibrillation
Description

Laparoscopic renal denervation system variant under development for atrial fibrillation treatment. Uses the same extravascular RDN approach as the core HyperQure system but targets cardiac arrhythmia applications in patients with recurrent AF following pulmonary vein isolation (PVI) and resistant hypertension.

Scale indicator7 records

Each record includes

Type, Value, Description, Source

Partnership10 partners
Strategic tierCoreTypeStrategic or Co-development Partner
Description

Stanford University is one of six leading US academic medical centers conducting DeepQure's IDE Early Feasibility Study for the HyperQure extravascular RDN system. Stanford is participating alongside Mayo Clinic, UC Irvine, University of Florida, Henry Ford Health System, and Emory University.

Strategic tierCoreTypeStrategic or Co-development Partner
Description

Mayo Clinic is one of six leading US academic medical centers conducting DeepQure's IDE Early Feasibility Study for HyperQure. Mayo Clinic is among the first institutions to receive IRB approval for the US clinical program.

Strategic tierCoreTypeStrategic or Co-development Partner
Description

UC Irvine was the site of the first US clinical procedure with the HyperQure device (January 17, 2025), performed by Professor Pengbo Jiang. UC Irvine was among the first institutions to grant IRB approval for DeepQure's US IDE clinical trial.

Strategic tierCoreTypeStrategic or Co-development Partner
Description

University of Florida is one of six leading US academic medical centers participating in DeepQure's IDE Early Feasibility Study for the HyperQure extravascular RDN system.

Strategic tierCoreTypeStrategic or Co-development Partner
Description

Henry Ford Health System is one of six US academic medical centers participating in DeepQure's US IDE Early Feasibility Study. Dr. Herbert Aronow, Medical Director of Heart & Vascular Service Line at Henry Ford Health, serves as a DeepQure advisor.

Strategic tierCoreTypeStrategic or Co-development Partner
Description

Emory University Medical Center is one of the US academic medical centers conducting DeepQure's US IDE Early Feasibility Study for the HyperQure extravascular RDN system.

Strategic tierCoreTypeStrategic or Co-development Partner
Description

University of Arizona is one of the seven US university hospitals planned for DeepQure's US clinical trial program for HyperQure, per the December 2024 announcement.

Strategic tierCoreTypeStrategic or Co-development Partner
Description

CBSET is a GLP-certified preclinical research facility that conducted large-animal (porcine) studies for DeepQure's FDA submission. Dr. Abraham Rami Tzafriri of CBSET presented 12-week safety and efficacy data for HyperQure at TCT 2024. CBSET's preclinical work supported FDA IDE approval for the HyperQure system.

9Multiple Global Medtech Companies (unnamed)
Strategic tierMinorTypeStrategic or Co-development Partner
Description

DeepQure has received strong interest from multiple major medtech firms and is in active discussions regarding strategic collaboration with one global medtech player for partnership and/or market development.

deepqure.com
Strategic tierCoreTypeStrategic or Co-development Partner
Description

DeepQure's Korean first-in-human clinical trial is conducted at Seoul National University Hospital (SNUH) and additional Korean institutions. Professor Chang-Wook Jeong, co-founder and CMO of DeepQure, is Professor of Urology at SNUH and led the research program that developed the HyperQure technology.

Recent move6 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight7 records

Each record includes

Type, Description

Peers10 records
TypeOthers
Description

Intuitive Surgical manufactures the da Vinci SP single-port robotic platform used to deploy HyperQure. Technology/integration partner rather than competitor; strategic relationship already demonstrated at UC Irvine.

TypeBroad incumbent
Description

Boston Scientific acquired SoniVie for $540M (March 2025) and is a likely acquirer of or strategic partner for DeepQure given its cardiovascular interventional portfolio and stated interest in RDN.

TypeBroad incumbent
Description

Otsuka acquired Recor Medical (~$800M, 2023) and is commercializing the Paradise RDN system globally. Diversified pharma-medtech incumbent with deep cardiovascular and renal portfolios; potential strategic partner for DeepQure.

TypeEmerging player
Description

Cala Health develops non-invasive wearable neuromodulation therapies (TAPS therapy) for hypertension and tremor. Adjacent emerging player pursuing device-based hypertension treatment via a different mechanism.

TypeDirect peer
Description

SoniVie developed an intravascular ultrasound RDN system and was acquired by Boston Scientific for $540M in March 2025. Closest extravascular-adjacent competitor and a key valuation/acquisition comparable for DeepQure.

TypeDirect peer
Description

Medtronic markets Symplicity Spyral, the leading FDA-approved catheter-based renal denervation system. Direct competitor to DeepQure in treating resistant hypertension via RDN; DeepQure's clinical differentiation is benchmarked against Symplicity Spyral's ~5.4 mmHg BP reduction.

TypeDirect peer
Description

Recor's Paradise ultrasound RDN system is FDA-approved for hypertension and competes head-to-head with DeepQure's HyperQure. Acquired by Otsuka in 2023 (~$800M); directly comparable efficacy benchmark (Paradise shows ~8.5 mmHg reduction).

TypeEmerging player
Description

Kona Medical is pursuing non-invasive externally-delivered ultrasound RDN for hypertension. Earlier-stage competitor with a different delivery mechanism but overlapping target indication.

TypeEmerging player
Description

Mercator is developing catheter-based micro-infusion RDN (Bullfrog system) for hypertension. Earlier-stage competitor with overlapping indication but different delivery modality.

TypeEmerging player
Description

Ablative Solutions is developing a percutaneous chemical RDN approach (Peregrine System) for resistant hypertension. Smaller, earlier-stage competitor focused on a different energy modality but the same hypertension indication.

Market position
Strengths5 records

Each record includes

Headline, Details, Source

Weaknesses5 records

Each record includes

Headline, Details, Source

Competitive moat4 records

Each record includes

Type, Details

Key risks7 records

Each record includes

Headline, Details, Source

Key highlights7 records

Each record includes

Headline, Details, Source

Customer concentration

Classification, Details

Segment1 record

Each record includes

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

Ideal customer profile1 record

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

Feature7 records

Each record includes

Title, Differentiator, Description, Source

Core technology
Revenue estimate
Valuation estimate
Number of profiles
Profiles9 records

Each record includes

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

No data
Compliance4 records

Each record includes

Name, Class, Description

Funding overview

Funding stage, Last funding date, Total funding USD

Funding rounds1 record

Each record includes

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

Investors1 record

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 →

DeepQure

Renal Denervation Medical Devicesdeepqure.com

DeepQure is a clinical-stage Korean medical device company developing HyperQure, the world's first laparoscopic extravascular renal denervation system for treating resistant hypertension, with an expanding pipeline into atrial fibrillation.

What DeepQure does

DeepQure Inc. is a Seoul, South Korea-based clinical-stage medical device company developing HyperQure, the world's first laparoscopic extravascular renal denervation (RDN) system for the treatment of resistant hypertension. The company's core technology delivers temperature-controlled radiofrequency (RF) energy from outside the renal artery using a segmented electrode tip that wraps circumferentially around the vessel, enabling complete 360-degree denervation regardless of nerve distribution. Three electrode sizes address renal arteries ranging from 2mm to 11mm in diameter, covering branched and accessory arteries that catheter-based intravascular RDN systems cannot reach. The system is compatible with both laparoscopic and robotic (da Vinci SP single-port) surgical platforms and comprises a generator base unit, a shaft and electrode assembly, and a surgeon-controlled handle with safety features including an emergency release system.

The company originated from government-funded research initiated by co-founder Dr. Chang-Wook Jeong at Seoul National University Hospital and was incorporated as DeepQure Inc. DeepQure is currently conducting first-in-human trials in Korea (10 patients enrolled, completed December 2025) and an Early Feasibility Study across six leading US academic medical centers (Stanford, Mayo Clinic, Emory, UC Irvine, University of Florida, Henry Ford Health), with IRB approvals secured. The company has filed 170+ patents across more than 10 countries, received MFDS Breakthrough Device Designation (Innovative Medical Device No. 36, July 2023), and FDA Investigational Device Exemption approval (June 2024). The pipeline extends beyond hypertension to atrial fibrillation (MFDS cleared July 2025) and other sympathetic-mediated cardiovascular indications.

DeepQure's business model is anchored on direct enterprise sales of the HyperQure Class III medical device to hospital systems following FDA Pre-Market Approval and Korean MFDS clearance, with pricing benchmarked against industry RDN procedural costs of US$5,000-$10,000 per procedure. The company is also pursuing strategic collaboration with global medtech partners for potential co-development or market development. To date, DeepQure has raised approximately $18 million in total venture funding, most recently via a Series C round (April 2025) led by Sui Generis Partners (수이제네리스 파트너스). The company operates with a leadership team combining clinical innovators (CMO Dr. Jeong), finance executives (Chairman Chan-Ho Park, ex-Goldman Sachs/Warburg Pincus), and regulatory specialists (Global VP Jason G. Jones, ex-SoniVie), and has not yet generated commercial revenue.

DeepQure firmographics

Firmographics
Name
DeepQure
Legal name
DeepQure Inc.
Website
https://www.deepqure.com
Company type
Private
Founded year
2019
Operating status
Operating
Headcount range
1–10 employees
Short description
DeepQure is a clinical-stage Korean medical device company developing HyperQure, the world's first laparoscopic extravascular renal denervation system for treating resistant hypertension, with an expanding pipeline into atrial fibrillation.
Ownership category
akta.pro rank

Where DeepQure is headquartered

Location

Headquarters

HQ city
Seoul
HQ country
South Korea
HQ region
Asia

Offices1 record

Markets served

DeepQure business model

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

Revenue model

  1. Medical Device Hardware Sales: DeepQure is a clinical-stage medtech company developing and preparing to commercialize the HyperQure extravascular RDN system. As a Class III medical device targeting hospital-based interventional procedures, revenue will be generated through direct device sales to hospital systems following regulatory approval (FDA PMA / Korean MFDS). The company is also exploring strategic partnerships with global medtech firms.

Go-to-market motion1 record

Distribution channels1 record

Marketing channels6 records

DeepQure product offering

Product offering

Core offering

DeepQure is developing and preparing to commercialize the HyperQure system, the world's first laparoscopic extravascular renal denervation (RDN) device. It performs 360-degree circumferential RF ablation of renal nerves from outside the renal artery for treating resistant hypertension. The system consists of a Generator (RF energy source), Shaft and Electrode (surgical instrument with three electrode sizes for 2-11mm arteries), and Handle (surgeon control with safety features), and is compatible with laparoscopic and single-port robotic surgery.

Product overview

DeepQure offers HyperQure, the world's first laparoscopic extravascular renal denervation (RDN) system. The core HyperQure RDN System consists of three integrated components: a Generator (RF energy source), Shaft and Electrode (surgical instrument), and Handle (surgeon control interface). The system performs 360° circumferential nerve ablation from outside the renal artery using temperature-controlled RF ablation. A variant, HyperQure RDM System, is being developed for atrial fibrillation treatment. All products are currently in clinical trial stage.

Differentiator

Problem solved

Functional benefit

Brands

  • HyperQure: The world's first laparoscopic extravascular renal denervation (RDN) system designed for 360° circumferential ablation of renal nerves from outside the vessel. HyperQure is a next-generation RDN device targeting resistant hypertension and atrial fibrillation.

Products and services

  • HyperQure RDN System World's first laparoscopic extravascular renal denervation system that delivers radiofrequency energy from outside the renal artery for complete 360-degree circumferential nerve ablation. Consists of Generator (RF energy source and control unit), Shaft and Electrode (surgical instrument that wraps around the renal artery to deliver RF energy), and Handle (surgeon control interface with safety features). Designed for treating resistant hypertension in hospital-based interventional settings, with three electrode sizes covering renal arteries from 2mm to 11mm in diameter.
  • HyperQure RDM System Laparoscopic renal denervation system variant under development for atrial fibrillation treatment. Uses the same extravascular RDN approach as the core HyperQure system but targets cardiac arrhythmia applications in patients with recurrent AF following pulmonary vein isolation (PVI) and resistant hypertension.

Quantifiable outcome

  • 51 mmHg average reduction in systolic blood pressure at 12 months in Korean first-in-human study (baseline 165 mmHg to 114 mmHg)
  • +7 more outcomes

Companies that use DeepQure

Customer profile

Segments1 record

Ideal customer profiles1 record

DeepQure technology and API

Technology

Technology focussed Yes

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

Feature7 records

DeepQure partnerships and signals

Strategic signal

Partnerships

Ten partnerships are on record, tiered core and minor.

  • Stanford UniversitycoreStrategic or Co-development PartnerStanford University is one of six leading US academic medical centers conducting DeepQure's IDE Early Feasibility Study for the HyperQure extravascular RDN system. Stanford is participating alongside Mayo Clinic, UC Irvine, University of Florida, Henry Ford Health System, and Emory University.
  • Mayo CliniccoreStrategic or Co-development PartnerMayo Clinic is one of six leading US academic medical centers conducting DeepQure's IDE Early Feasibility Study for HyperQure. Mayo Clinic is among the first institutions to receive IRB approval for the US clinical program.
  • UC Irvine (University of California, Irvine)coreStrategic or Co-development PartnerUC Irvine was the site of the first US clinical procedure with the HyperQure device (January 17, 2025), performed by Professor Pengbo Jiang. UC Irvine was among the first institutions to grant IRB approval for DeepQure's US IDE clinical trial.
  • University of FloridacoreStrategic or Co-development PartnerUniversity of Florida is one of six leading US academic medical centers participating in DeepQure's IDE Early Feasibility Study for the HyperQure extravascular RDN system.
  • Henry Ford Health SystemcoreStrategic or Co-development PartnerHenry Ford Health System is one of six US academic medical centers participating in DeepQure's US IDE Early Feasibility Study. Dr. Herbert Aronow, Medical Director of Heart & Vascular Service Line at Henry Ford Health, serves as a DeepQure advisor.
  • Emory University Medical CentercoreStrategic or Co-development PartnerEmory University Medical Center is one of the US academic medical centers conducting DeepQure's US IDE Early Feasibility Study for the HyperQure extravascular RDN system.
  • University of ArizonacoreStrategic or Co-development PartnerUniversity of Arizona is one of the seven US university hospitals planned for DeepQure's US clinical trial program for HyperQure, per the December 2024 announcement.
  • CBSET (Center for Biomedical Science and Engineering Technology)coreStrategic or Co-development PartnerCBSET is a GLP-certified preclinical research facility that conducted large-animal (porcine) studies for DeepQure's FDA submission. Dr. Abraham Rami Tzafriri of CBSET presented 12-week safety and efficacy data for HyperQure at TCT 2024. CBSET's preclinical work supported FDA IDE approval for the HyperQure system.
  • Multiple Global Medtech Companies (unnamed)minorStrategic or Co-development PartnerDeepQure has received strong interest from multiple major medtech firms and is in active discussions regarding strategic collaboration with one global medtech player for partnership and/or market development.
  • Seoul National University HospitalcoreStrategic or Co-development PartnerDeepQure's Korean first-in-human clinical trial is conducted at Seoul National University Hospital (SNUH) and additional Korean institutions. Professor Chang-Wook Jeong, co-founder and CMO of DeepQure, is Professor of Urology at SNUH and led the research program that developed the HyperQure technology.

Scale indicators7 records

Recent moves6 records

Expansion highlights7 records

DeepQure competitors and assessment

Company assessment

Others

  • Intuitive Surgical: Intuitive Surgical manufactures the da Vinci SP single-port robotic platform used to deploy HyperQure. Technology/integration partner rather than competitor; strategic relationship already demonstrated at UC Irvine.

Broad incumbents

  • Boston Scientific: Boston Scientific acquired SoniVie for $540M (March 2025) and is a likely acquirer of or strategic partner for DeepQure given its cardiovascular interventional portfolio and stated interest in RDN.
  • Otsuka Holdings: Otsuka acquired Recor Medical (~$800M, 2023) and is commercializing the Paradise RDN system globally. Diversified pharma-medtech incumbent with deep cardiovascular and renal portfolios; potential strategic partner for DeepQure.

Emerging players

  • Cala Health: Cala Health develops non-invasive wearable neuromodulation therapies (TAPS therapy) for hypertension and tremor. Adjacent emerging player pursuing device-based hypertension treatment via a different mechanism.
  • Kona Medical: Kona Medical is pursuing non-invasive externally-delivered ultrasound RDN for hypertension. Earlier-stage competitor with a different delivery mechanism but overlapping target indication.
  • Mercator MedSystems: Mercator is developing catheter-based micro-infusion RDN (Bullfrog system) for hypertension. Earlier-stage competitor with overlapping indication but different delivery modality.
  • Ablative Solutions: Ablative Solutions is developing a percutaneous chemical RDN approach (Peregrine System) for resistant hypertension. Smaller, earlier-stage competitor focused on a different energy modality but the same hypertension indication.

Direct peers

  • SoniVie (Boston Scientific): SoniVie developed an intravascular ultrasound RDN system and was acquired by Boston Scientific for $540M in March 2025. Closest extravascular-adjacent competitor and a key valuation/acquisition comparable for DeepQure.
  • Medtronic: Medtronic markets Symplicity Spyral, the leading FDA-approved catheter-based renal denervation system. Direct competitor to DeepQure in treating resistant hypertension via RDN; DeepQure's clinical differentiation is benchmarked against Symplicity Spyral's ~5.4 mmHg BP reduction.
  • Recor Medical (Otsuka): Recor's Paradise ultrasound RDN system is FDA-approved for hypertension and competes head-to-head with DeepQure's HyperQure. Acquired by Otsuka in 2023 (~$800M); directly comparable efficacy benchmark (Paradise shows ~8.5 mmHg reduction).

Market position

Strengths5 records

Weaknesses5 records

Competitive moat4 records

Key risks7 records

Key highlights7 records

Customer concentration

DeepQure social profiles

Digital presence

DeepQure compliance and trust

Trust signal

Compliance4 records

DeepQure financial estimates

Financial estimate

Revenue estimate

Valuation estimate

DeepQure leadership team

Management profile

Number of profiles

Profiles9 records

DeepQure funding detail

Funding detail

Funding overview

Funding rounds1 record

Investors1 record

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

DeepQure 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 DeepQure

What does DeepQure do?

DeepQure is developing and preparing to commercialize the HyperQure system, the world's first laparoscopic extravascular renal denervation (RDN) device. It performs 360-degree circumferential RF ablation of renal nerves from outside the renal artery for treating resistant hypertension. The system consists of a Generator (RF energy source), Shaft and Electrode (surgical instrument with three electrode sizes for 2-11mm arteries), and Handle (surgeon control with safety features), and is compatible with laparoscopic and single-port robotic surgery.

Is DeepQure a public or private company?

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

When was DeepQure founded?

DeepQure was founded in 2019. It employs 1 to 10 people.

Where is DeepQure based?

DeepQure is headquartered in Seoul, South Korea, in the Asia region.

How does DeepQure make money?

One revenue line is on record: medical Device Hardware Sales.

Who are DeepQure's main competitors?

Intuitive Surgical is listed as an others. Broad incumbents are Boston Scientific and Otsuka Holdings. Emerging players are Cala Health, Kona Medical, Mercator MedSystems and Ablative Solutions. Direct peers are SoniVie (Boston Scientific), Medtronic and Recor Medical (Otsuka).

Does DeepQure have an API?

No public API is recorded for DeepQure.

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Live signals
PR NewswireDeepQure Announces Robust 3-Month Results from HERO-HTN Clinical Study at EuroPCR 2026DeepQure announced robust 3-month interim clinical data from its HERO-HTN-FIH study at EuroPCR 2026, demonstrating that the HyperQure™ extravascular renal denervation system achieved significant blood pressure reductions with a median drop of 25.0 mmHg in 24-hour ambulatory systolic blood pressure and 39.5 mmHg in office systolic blood pressure. The study reported zero device-related major adverse events and showed that 70% of patients reached target blood pressure below 140 mmHg, while the median number of antihypertensive medications per patient decreased from 6.0 to 4.5. The company indicated it is in active discussions with the FDA and preparing to launch a Global Pivotal Study following successful completion of 15 cases at U.S. institutions including Stanford University and Mayo Clinic.PR Newswire APACDeepQure Announces Robust 3-Month Results from HERO-HTN Clinical Study at EuroPCR 2026DeepQure announced 3-month results from its HERO-HTN-FIH study at EuroPCR 2026, showing a median 25.0 mmHg reduction in 24-hour ambulatory systolic blood pressure and 39.5 mmHg in office systolic blood pressure. The study met all primary efficacy and safety endpoints, with 70% of patients achieving target blood pressure and zero device-related major adverse events.PR NewswireDeepQure Reports Encouraging Clinical Data from World's First Extravascular RDN System at AUA 2026DeepQure presented clinical progress for HyperQure, its extravascular renal denervation system for uncontrolled hypertension, at the AUA 2026 Innovation Nexus Forum in Washington. The company reported completing 15 cases across Korea's first-in-human trial and the US Early Feasibility Study with no device-related major adverse events reported. Full clinical data is scheduled for presentation at EuroPCR 2026, and DeepQure is now focused on advancing its global pivotal trial.openPR.comAtrial Fibrillation Pipeline 2026: Key Companies, MOA, ROA, and Clinical Trials Evaluation by DelveInsight | Bayer, Johnson and Johnson, Bristol Myers-Squibb, Daiichi Sankyo, Pfizer, Anthos TherapDelveInsight Business Research LLP published a market research report identifying 12+ companies developing 15+ therapies for atrial fibrillation treatment, with candidates in various clinical stages from preclinical to Phase III. In December 2025, the U.S. Food and Drug Administration approved Abbott's Volt PFA System for treating atrial fibrillation, following its earlier CE Mark authorization in the European Union. In July 2025, South Korea's Ministry of Food and Drug Safety granted DeepQure approval to conduct a clinical trial of its HyperQure RDM System, a laparoscopic renal denervation technology for atrial fibrillation.PR NewswireDeepQure Strengthens Clinical Leadership with Former SoniVie Executive AppointmentDeepQure, a South Korea-based medical technology company, announced the appointment of Jason G. Jones as Global Vice President of Clinical & Regulatory Affairs to accelerate its HyperQure™ renal denervation system development. Jones joins from SoniVie, an Israeli company recently acquired by Boston Scientific for $540 million in March 2025, where he led clinical development strategy and completed enrollment for their Early Feasibility Study. The appointment is expected to strengthen DeepQure's ongoing global clinical trial and advance commercialization of its extravascular RDN technology targeting resistant hypertension.PR NewswireDeepQure Presents Clinical Results of Laparoscopic RDN at TCT 2024, Demonstrating Cutting-edge Technology and InnovationDeepQure presented clinical results of its laparoscopic renal denervation device "HyperQure" at TCT 2024 in Washington, D.C., reporting that six hypertensive patients have been successfully treated in an ongoing domestic clinical trial initiated in January, with four more patients expected to enroll before year-end. CBSET, the GLP-certified research facility that conducted preclinical animal studies, also presented 12-week safety and efficacy data supporting the device's FDA Investigational Device Exemption approval. The company announced it will launch global clinical trials in November following these positive outcomes.