Cart.

No products in the cart.

NeoGen nitrogen plasma skin regeneration machine with digital touchscreen interface.
NeoGen professional plasma aesthetics device on mobile trolley with handpiece.
Side-profile view of the NeoGen plasma machine on a wheeled base.
NeoGen nitrogen plasma skin regeneration machine with digital touchscreen interface.
NeoGen professional plasma aesthetics device on mobile trolley with handpiece.
Side-profile view of the NeoGen plasma machine on a wheeled base.

Neogen

Neogen

Description

Structural skin regeneration for facial volume loss. Restores dermal architecture for the growing post-weight loss patient demographic.

Neogen utilizes controlled nitrogen plasma energy to remodel dermal tissue from within, preserving the epidermal barrier while generating deep neocollagenesis and elastogenesis. FDA cleared across 7 clinical indications.

FDA Cleared Badge
Explore the Artemis payment program -

The post-weight-loss aging wave.
As GLP-1 medications reach unprecedented scale, a surge of patients seeks solutions for rapid volume loss. NeoGen rebuilds dermal architecture from within to meet this demand.

A different kind of aging.
Rapid fat loss often accelerates the depletion of collagen and elastin. This leads to hollowing and deflation reflecting deep structural changes that the NeoGen specifically targets.

Clinically proven density.
Neogen is a non-invasive regenerative facial technology. It is clinically shown to increase skin density by 80%, restoring firmness and resilience from within.

Beyond fractional lasers.
Neogen delivers natural restoration by regenerating volume in a way that tightening treatments, injections, and lasers cannot.
Neogen plasma treatment: 4 months after treatment
4 months after treatment.
Neogen plasma treatment: 3 months after treatment
3 months after treatment.
Neogen plasma treatment: 2 weeks after medium energy treatment
2 weeks after medium energy treatment.
Neogen plasma treatment: 2 weeks after treatment
2 weeks after treatment.
"We had our Neogen device for over six months and did around $107k, but we were stuck in a 'one-and-done' high-energy mindset that our providers weren't fully confident delivering. Once we connected with Kate and the Artemis team, everything changed. We shifted to customized treatment packages and deeper patient conversations, and the energy in the clinic completely took off—our team is confident, retail is stronger, and we generated nearly $71k in less than two months. Partnering with a team that actually guides your commercial strategy is a game changer."
Lisa
Derm Loft

Download full technical specifications (PDF).

Dimensions: Generator only. Height. 10.2 inches.
Width. 18.5 inches.
Depth. 19.7 inches (ex. connectors).
Dimensions: Overall. Height. 46.5 inches.
Width. 18.5 inches.
Depth. 23.1 inches.
Weight. Generator section only. 40 lbs.
Trolley section only. 35 lbs.
Overall (including regulator and 2x cylinders of the suggested type). 75 lbs.
Power requirements. Voltage:
1. Nominal operating range.
2. Min-max operating limits.		 1. 100–230 AC Vrms, single phase.
2. 90–264 AC Vrms.
Current. 6.5 A max.
Frequency. 50/60 Hz.
Power consumption. ≤650 VA.
Gas.

Please note: The gas pressure regulator requires inspection at 12-month intervals. Contact support@artemis.co for more information.

 Type & grade. Pharmaceutical or instrument grade nitrogen.
Minimum purity. 99.5%.
Suggested type. Air Liquide T4514-ED2 (560L) (with CGA-580 fitting).
Warning: Do not use any other type of gas or any other grade of nitrogen.
Cylinder size (max). Height: 25.5 in.
Diameter: 5.12 in.
Regular fitting. CGA580 (standard).
BS3 (optional).
Gas pressure regulator. Included with the Neogen system. 2-stage pressure regulator with solid-state gas cylinder pressure sensor, over-pressure relief valve (3 bar gauge), outlet flow restrictor (5 litres/min), and flexible hose with releasable self-sealing valve connection to the generator.
Cylinder pressure (max) / regulator outlet pressure. 3000 psi / 1.7 bar (nom.).
Neogen system output. Output. Pulsed nitrogen plasma.
A: With 5 mm disposable nozzle fitted, measured with a 5.0 +/-0.5 mm separation between the instrument nozzle and the measuring surface:
Energy delivered to patient. 1 to 4 J per plasma pulse.
Power delivered to patient. 1 Watt min. (1 J, 1 Hz) 10 Watts max (4 J, 2.5 Hz).
B: With 25 mm disposable nozzle fitted, measured with a 25.0 +/-1 mm separation between the instrument nozzle and the measuring surface:
Energy delivered to patient. 0.5 to 0.8 J per plasma pulse.
Power delivered to patient. 0.5 Watt min. (0.5 J, 1 Hz) 2 Watts max (0.8 J, 2.5 Hz).
Safety. Classification. Class 1 per BS EN 60601-1:2006.
Earthing (grounding). Protective earth (ground) connection is required.
Applied part classification. Type BF (not defibrillator proof).
MDD class. IIb.
FDA regulation number. 21 CFR 878.4400.
FDA regulation name. Electrosurgical cutting and coagulation device and accessories.
FDA product code. GEI.
FDA 510(k) reference. K221873.
RF output.

Please note: Neogen is not an RF device or treatment. RF energy is used only within the handpiece to convert the liquid nitrogen into plasma energy. No RF energy is delivered into the skin during this treatment.

 Frequency. 2470 MHz typ.
(2450 to 2480 MHz).
Output power:
Nominal.
Peak.		 1300 Watts.*
1700 Watts.
Average across a pulse into 50 Ohms, measured at the generator output socket.
Modulation. Pulsed CW (carrier wave).
Pulse repetition rate (repeat pulse mode). 5.2 to 15.4 ms.
Pulse width. (1.0 to 2.5 Hz).
Output protection. Automatic shutdown occurs following detection of a number of fault conditions including absence of plasma detected through optical means in the handpiece.

Output is disabled temporarily following detection of other conditions such as absence of a disposable tip or attempted use of a disposable tip beyond its rated lifetime.
Environmental limits: System transport and storage. Ambient temperature. 0 to 40°C.
Relative humidity. 10% to 90% non-condensing.
Atmospheric pressure. 500 to 1060 hPa.
Environmental limits: System operation. Ambient temperature. 10 to 30°C.
Relative humidity. 30 to 75% non-condensing.
Atmospheric pressure. 700 to 1060 hPa.

The post-weight-loss aging wave.
As GLP-1 medications reach unprecedented scale, a surge of patients seeks solutions for rapid volume loss. NeoGen rebuilds dermal architecture from within to meet this demand.

A different kind of aging.
Rapid fat loss often accelerates the depletion of collagen and elastin. This leads to hollowing and deflation reflecting deep structural changes that the NeoGen specifically targets.

Clinically proven density.
Neogen is a non-invasive regenerative facial technology. It is clinically shown to increase skin density by 80%, restoring firmness and resilience from within.

Beyond fractional lasers.
Neogen delivers natural restoration by regenerating volume in a way that tightening treatments, injections, and lasers cannot.

Neogen plasma treatment: 4 months after treatment
4 months after treatment.
Neogen plasma treatment: 3 months after treatment
3 months after treatment.
Neogen plasma treatment: 2 weeks after medium energy treatment
2 weeks after medium energy treatment.
Neogen plasma treatment: 2 weeks after treatment
2 weeks after treatment.

"We had our Neogen device for over six months and did around $107k, but we were stuck in a 'one-and-done' high-energy mindset that our providers weren't fully confident delivering. Once we connected with Kate and the Artemis team, everything changed. We shifted to customized treatment packages and deeper patient conversations, and the energy in the clinic completely took off—our team is confident, retail is stronger, and we generated nearly $71k in less than two months. Partnering with a team that actually guides your commercial strategy is a game changer."
Lisa
Derm Loft

Download full technical specifications (PDF).

Dimensions: Generator only. Height. 10.2 inches.
Width. 18.5 inches.
Depth. 19.7 inches (ex. connectors).
Dimensions: Overall. Height. 46.5 inches.
Width. 18.5 inches.
Depth. 23.1 inches.
Weight. Generator section only. 40 lbs.
Trolley section only. 35 lbs.
Overall (including regulator and 2x cylinders of the suggested type). 75 lbs.
Power requirements. Voltage:
1. Nominal operating range.
2. Min-max operating limits.		 1. 100–230 AC Vrms, single phase.
2. 90–264 AC Vrms.
Current. 6.5 A max.
Frequency. 50/60 Hz.
Power consumption. ≤650 VA.
Gas.

Please note: The gas pressure regulator requires inspection at 12-month intervals. Contact support@artemis.co for more information.

 Type & grade. Pharmaceutical or instrument grade nitrogen.
Minimum purity. 99.5%.
Suggested type. Air Liquide T4514-ED2 (560L) (with CGA-580 fitting).
Warning: Do not use any other type of gas or any other grade of nitrogen.
Cylinder size (max). Height: 25.5 in.
Diameter: 5.12 in.
Regular fitting. CGA580 (standard).
BS3 (optional).
Gas pressure regulator. Included with the Neogen system. 2-stage pressure regulator with solid-state gas cylinder pressure sensor, over-pressure relief valve (3 bar gauge), outlet flow restrictor (5 litres/min), and flexible hose with releasable self-sealing valve connection to the generator.
Cylinder pressure (max) / regulator outlet pressure. 3000 psi / 1.7 bar (nom.).
Neogen system output. Output. Pulsed nitrogen plasma.
A: With 5 mm disposable nozzle fitted, measured with a 5.0 +/-0.5 mm separation between the instrument nozzle and the measuring surface:
Energy delivered to patient. 1 to 4 J per plasma pulse.
Power delivered to patient. 1 Watt min. (1 J, 1 Hz) 10 Watts max (4 J, 2.5 Hz).
B: With 25 mm disposable nozzle fitted, measured with a 25.0 +/-1 mm separation between the instrument nozzle and the measuring surface:
Energy delivered to patient. 0.5 to 0.8 J per plasma pulse.
Power delivered to patient. 0.5 Watt min. (0.5 J, 1 Hz) 2 Watts max (0.8 J, 2.5 Hz).
Safety. Classification. Class 1 per BS EN 60601-1:2006.
Earthing (grounding). Protective earth (ground) connection is required.
Applied part classification. Type BF (not defibrillator proof).
MDD class. IIb.
FDA regulation number. 21 CFR 878.4400.
FDA regulation name. Electrosurgical cutting and coagulation device and accessories.
FDA product code. GEI.
FDA 510(k) reference. K221873.
RF output.

Please note: Neogen is not an RF device or treatment. RF energy is used only within the handpiece to convert the liquid nitrogen into plasma energy. No RF energy is delivered into the skin during this treatment.

 Frequency. 2470 MHz typ.
(2450 to 2480 MHz).
Output power:
Nominal.
Peak.		 1300 Watts.*
1700 Watts.
Average across a pulse into 50 Ohms, measured at the generator output socket.
Modulation. Pulsed CW (carrier wave).
Pulse repetition rate (repeat pulse mode). 5.2 to 15.4 ms.
Pulse width. (1.0 to 2.5 Hz).
Output protection. Automatic shutdown occurs following detection of a number of fault conditions including absence of plasma detected through optical means in the handpiece.

Output is disabled temporarily following detection of other conditions such as absence of a disposable tip or attempted use of a disposable tip beyond its rated lifetime.
Environmental limits: System transport and storage. Ambient temperature. 0 to 40°C.
Relative humidity. 10% to 90% non-condensing.
Atmospheric pressure. 500 to 1060 hPa.
Environmental limits: System operation. Ambient temperature. 10 to 30°C.
Relative humidity. 30 to 75% non-condensing.
Atmospheric pressure. 700 to 1060 hPa.

You may also like

FAQs

Neogen was developed specifically to address structural facial changes commonly seen after rapid weight loss. Practices treating post-weight-loss medication patients often find it particularly relevant, though suitability is discussed during the qualification call.

Neogen is designed to complement existing services. Many practices position it as a regenerative option for patients who aren’t ideal candidates for tightening-only treatments, fillers, or ablative lasers.

Neogen is supported by Artemis with training and onboarding designed to integrate smoothly into established practice workflows. Details are reviewed during the application process.

As weight-loss medication use continues to rise, many practices report increasing interest from patients seeking solutions for improvement in facial volume after weight loss. Neogen was developed in response to this growing demand.