Our Technology

Cold plasma.
Localized. Transient.
Broad-spectrum.

Aceso Plasma is a handheld, portable device that generates a transient, localized plasma field from ambient air. The multifactorial device outputs — including localized electric-field effects, charged particles, photons, and short-lived reactive species generated in situ — support wound-bed preparation and wound environment management. Based on FDA guidelines for thermal injury, the device does not cause irreversible thermal injury when used as directed.

O₂
Ambient air input
Plasma field
O⁻
Ionized gas
Device outputs
Reduced microbial and biofilm burden
Operates from ambient air — no external tanks required Safe for patients and operators AC or DC powered Low-temperature operation — no thermal damage Minimal antibiotic resistance risk
Aceso Plasma handheld device — converts ambient air into oxygen plasma
Investigational device
Pending FDA clearance · Not for sale
Important: Aceso Plasma is an investigational device currently pending FDA clearance. This device is not approved or available for clinical use or sale.
The science

How it works

Aceso Plasma field outputs — transient, multifactorial, localized plasma field diagram
Investigational evidence

Validated across
five institutions

Aceso Cold Plasma has been evaluated across five independent research institutions — including Wake Forest Institute of Regenerative Medicine, MedStar Georgetown Research Institute, and the US Army CCDC CBC. Investigational studies observed reduced microbial bioburden, accelerated wound healing in pre-clinical models, and a favorable safety profile at the treatment durations tested. Characterization of tissue effects and clinical outcomes is ongoing.

MedStar Georgetown Research Institute — demonstrated antimicrobial activity across 14+ pathogen species including antibiotic-resistant ESKAPE strains, comparable to Povidone Iodine at tested durations.

Wake Forest Institute of Regenerative Medicine — in vivo wound studies observed reduced wound contraction and accelerated re-epithelization in plasma-treated groups compared to untreated controls.

MedStar Georgetown — Burn Wound Study — porcine burn models showed reduced bioburden and no adverse impact on healing trajectory at the treatment parameters tested.

Technology pillars

What makes Aceso Plasma different

Five core technology advantages that set Aceso Plasma apart from conventional wound care and disinfection approaches — in both clinical and field environments.

Multifactorial plasma outputs

Device-generated plasma produces transient, localized outputs — including reactive species generated in situ — that are scientifically recognized as capable of reducing microbial bioburden under defined experimental conditions.

Cold plasma technology

Operates at low temperatures — safely treating delicate tissues without thermal damage. Delivers power of plasma without the harmful side effects associated with heat-based or chemical approaches. Treatment parameters are designed to stay within a safe treatment window.

Operates from ambient air

The device draws from ambient air as its input — requiring no external gas tanks. Environmentally clean and logistically simple — critical for austere field deployment.

Portable power

Powered by AC or DC, the device operates across clinical settings and austere field environments without sacrificing output. Lightweight, hand-portable, and ready to deploy where it's needed most.

Versatile applications

Adaptable across wound healing, infected wounds, and equipment decontamination — in clinical, surgical, dermatological, and military field settings.

Pipeline & Milestones

From research to
clinical reality.

Aceso Plasma has built a foundation of independently validated research, government-funded development, and strategic investment. Here's where we've been — and where we're going.

Forward-looking statements: Upcoming milestones represent current plans and targets. Actual results and timelines may differ materially from those projected.

Development stage

Pre-Clinical Research

Completed 2022

SBIR Funding

Phase I & II complete

Series A Initial Tranche

Closed July 2025

V2 Development & FDA Submission

In progress · 2026

Clinical Trials & FDA Clearance

Upcoming

Aceso Plasma is an investigational device. The device is not currently cleared or approved for clinical use.

A track record of
delivering on commitments.

From the first government order to SBIR completion and the closing of our initial Series A tranche — every milestone delivered on time and on budget.

2020

January

Defense

Device Units Delivered to Government Agency

Delivered two Aceso Plasma Generator units to a government agency under a research and evaluation agreement — demonstrating early government interest in the technology and its potential field applications.

2020

Feb – Jun

Funding

SBIR Phase I & Phase II Awarded — $1.55M

Awarded $1.55M in combined SBIR Phase I and Phase II funding by the US Air Force to conduct research studies across wound healing, antimicrobial efficacy, burn wound care, and chemical agent decontamination.

2022

February

Research

All Four SBIR Research Studies Completed

Completed four independent research studies — all on time and on budget — at Wake Forest Institute of Regenerative Medicine, MedStar Georgetown Research Institute, US Army CCDC CBC, and Edgewood Chemical Biological Center. Results established a comprehensive pre-clinical evidence base across wound healing, disinfection, burn care, and CBRN decontamination.

2025

July

Investment

Series A Initial Tranche Closed — Led by Stony Lonesome Group

Successfully closed the initial tranche of our Series A Preferred financing, led by Stony Lonesome Group — a proven early-stage defense and dual-use investor with 14 years of mission-focused investment. Funding supports the next phase of clinical development, regulatory advancement, and production development.

Read announcement on Soldier Systems Daily

Active development
across four fronts.

Four parallel workstreams are underway in 2026 — advancing the device, the regulatory pathway, and the clinical leadership team simultaneously.

2026

June

Product Development

Version 2 Prototypes — Device & Tips

Contract manufacturer Synectic is completing Version 2 prototypes for both the Aceso Plasma Generator and its interchangeable tips. Testing is scheduled to begin immediately upon completion — including spectroscopy, petri dish, and animal laboratory evaluations to validate performance improvements.

In progress

2026

June

Regulatory

FDA Breakthrough Designation Submission

Preparing a Breakthrough Device Designation submission to the FDA. If received, Breakthrough Designation will provide clarity on the regulatory pathway, facilitate more frequent interaction with the FDA during development, and create significant marketing and credibility opportunities for the company.

Submission being prepared

2026

May

Leadership

Chief Medical Officer Appointed — Dr. Trip Johnson

Dr. Trip Johnson, a retired physician from the Joint Medical Augmentation Unit (JMAU), has joined Aceso Plasma as Chief Medical Officer. Dr. Johnson brings deep experience in military medicine and special operations medical support, and will chair the company's newly forming Physician Advisory Board.

Completed

2026

2026

Clinical

Physician Advisory Board — Formation Underway

Identifying candidates for a 2-3 physician Physician Advisory Board to be chaired by CMO Dr. Trip Johnson. The board will advise on strategic clinical issues, help communicate the unmet needs in current wound care, and guide Aceso's clinical positioning as the company advances toward FDA clearance.

Candidates being identified

The road to
FDA clearance.

The following milestones represent Aceso Plasma's current development roadmap. Timelines are targets and subject to change.

TBD

Upcoming

Clinical

Clinical Trials — MedStar Georgetown Research Institute

Clinical trials are set to begin at MedStar Georgetown Research Institute for chronic wounds and ESKAPE pathogen-infected wounds — the primary FDA clearance pathway for the Aceso Plasma Generator.

TBD

Upcoming

Regulatory

ESKAPE Pathogen Animal Study

Infected wound healing animal study focused on ESKAPE pathogens — providing additional pre-clinical data to support the FDA De Novo application for the chronic wound care indication.

TBD

Upcoming

Regulatory

FDA Clearance — Chronic Wound Care Indication

Pursuing FDA De Novo clearance for the chronic wound care indication — the primary commercial pathway enabling clinical adoption across wound care centers, hospitals, and surgical settings.

TBD

Upcoming

Defense

Decon Chamber — Engineering & High-Level Disinfection Certification

Advancing the Aceso Decontamination Chamber from proof-of-concept prototype to engineered product, targeting FDA High-Level Disinfection Certification for use in military and medical settings.

In the news

Third-party recognition of our progress.

Soldier Systems Daily · July 2025

"Aceso Plasma Inc., which develops cold plasma medical and decontamination technology, today announced it has successfully closed a Series A Preferred funding round... led by Stony Lonesome Group, LLC. This milestone will support the next phase of clinical trials, regulatory advancement, and production development."

Sean Drake, Founder — Stony Lonesome Group: "Founded by former Navy SEALs, the company exemplifies the kind of veteran-led innovation that Stony Lonesome Group has championed for over 14 years through our Mission-Focused investment thesis."

Read full article
Invest in the mission

Interested in
where we're headed?

We are actively building relationships with accredited investors, clinical partners, and military collaborators. If you'd like to learn more about Aceso Plasma's development roadmap, we'd love to connect.

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