About

About Medfiniti

Medfiniti is a medical technology platform company built around treatment technology, recurring procedure-based revenue, and disciplined operating execution.

Company Overview

Not a device company. A platform company.

Medfiniti is organized as a medical technology platform company rather than a single-product device manufacturer. The company integrates intellectual property, operating infrastructure, and clinical deployment within a unified structure designed to support recurring revenue and long-term platform development.

Its current operating platform, HemWell MD, serves as the company's initial commercial proof point and operating foundation for future growth.

Incorporated
2017 (Medfiniti)
Headquarters
United States
Current Platform
HemWell MD
Technology Origin
Direct Current Electrolysis
Gen 2 Launch
February 2026
Structure
Medical Technology Platform Company
Operating Proof

Current operating scale

40,000+
Procedures Performed
51
Active Centers
Per-Use / Free Device
Commercial Model
History

From Ultroid to Medfiniti

The current Medfiniti platform originated from direct current electrolysis technology first developed in the late 1990s. Following the acquisition of the technology and patents in 2021, Medfiniti rebuilt the operating model, device architecture, quality systems, and commercialization approach into the platform in place today.

Late 1990s–2015

Ultroid Technology Era

Direct current electrolysis technology developed, receiving CE approval (1996) and FDA clearance (1999). Successfully deployed in clinical practice for over 15 years, treating an estimated 155,000+ procedures.

2017

Medfiniti, Inc. Founded & IP Acquired

Medfiniti, Inc. incorporated and acquired the core intellectual property and patent portfolio. The company began comprehensive restructuring, including quality system remediation and regulatory pathway development.

2017–2019

Gen 1 R&D

HemWell MD created. Complete redesign of device architecture, quality management systems, and operating model, culminating in FDA 510(k) clearance.

2020

Gen 1 Trial Launch

Gen 1 device launched, introducing the initial commercialization framework and beginning clinical deployment.

2022–2025

Gen 2 R&D and Corporate Platform Reorganization

Development of enhanced Gen 2 device architecture, incorporating connectivity improvements, updated platform infrastructure, and expanded clinical capabilities. Medfiniti, Inc. underwent a corporate reorganization to establish its current platform architecture: Medfiniti, Inc. (Parent) → Medfiniti IP, LLC (IP) → HemWell MD International, Inc. (Global Management) → regional operating subsidiaries (HemWell MD, Inc. – North America, HemWell MD GOV – Government & Military, HemWell MD B.V. – E.U./U.K., HemWell MD GCC – Middle East).

February 2026

Gen 2 Trial Launch and Replacement of Gen 1s

HemWell Gen 2 launched nationally in February 2026 with enhanced device architecture and connectivity. Full replacement of Gen 1 systems underway across 51 active centers with 40,000+ cumulative procedures performed.

Q3 2026

Government & Military Launch — VA Hospitals

HemWell MD GOV is launching its Government & Military division in Q3 2026, targeting VA Hospital systems across the United States. This initiative brings the HemWell MD procedure to veterans through an established government contracting framework.

2027 Forward

Platform Expansion — Middle East, EU & Gen 3

Medfiniti is targeting the commercial launch of HemWell MD B.V. across the European Union and HemWell MD GCC across the Middle East in 2027, leveraging established regional management and regulatory pathways. In parallel, Gen 3 is in development and planned to revolutionize hemorrhoid treatment through a completely new delivery system — designed to expand the total addressable market 8–10x while extending operating, data, and clinical capabilities.

Operating Evolution

Why the current model works

Medfiniti's current operating success reflects more than inherited technology. It reflects changes in procedure design, reimbursement alignment, customer targeting, device architecture, and business model.

Procedure Model

The current platform incorporates anesthesia and a one-and-done treatment concept, improving patient completion and reducing the need for multiple return visits.

Coding and Reimbursement

The operating model is structured around appropriate use of CPT ligation codes, improving the commercial viability of the procedure for physician practices.

Target Customer

HemWell MD is commercialized primarily to gastroenterologists, rather than the earlier physician targeting strategy used by the predecessor system.

Technology Platform

The Gen 2 device introduced updated technology architecture, including connectivity enhancements and a stronger foundation for future platform development.

Business Model

The company provides the device without upfront capital cost and monetizes through per-procedure usage, materially changing the adoption model relative to the predecessor system.

Leadership

Our team

Michael J. Goeree, MBA

Michael J. Goeree, MBA

CEO / Chairman

Medfiniti, Inc.

Stephen Goldman, MD, FACC

Stephen Goldman, MD, FACC

CMO / Vice Chairman

Medfiniti, Inc.

Matt Totty

Matt Totty

Chief Financial Officer

Medfiniti, Inc.

Cedric E. Lewis, JD, MBA

Cedric E. Lewis, JD, MBA

President / Governance

Medfiniti IP, LLC

Reed Hogan III, MD, FACG

Reed Hogan III, MD, FACG

Medical Director

HemWell MD International

Mitch Weiner

Mitch Weiner

VP Sales

HemWell MD

Clyde Hubbard

Clyde Hubbard

President & Managing Director

HemWell MD GOV

Harro Schulz, LL.M.

Harro Schulz, LL.M.

International Executive Director

HemWell MD B.V. (Europe & GCC)

Samantha Paolitto

Samantha Paolitto

Administrative Director

Medfiniti, Inc.

Position
Medfiniti is building a platform company around clinical technology, operating infrastructure, and recurring procedure-based economics.

Current operating platform: HemWell MD