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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

$99,000.00

Description

7 FDA indications. 80% density increase. One regenerative breakthrough.

Neogen is the ultimate non-invasive solution for structural skin regeneration—trusted worldwide and FDA-cleared for professional use. This advanced system utilizes nitrogen plasma technology to rebuild the skin’s underlying architecture from within – delivering visible volume and firmness.

  • Rebuild Structure: Stimulates collagen plus demonstrated elastin remodeling.
  • Proven Safe: Seven FDA clearances for skin types one-four.
  • GLP-1 Solution: Restores volume loss and facial hollowing concerns.
  • Non-Ablative: Reaches reticular dermis while keeping surface intact.
  • Visible Results: Restores natural fullness and density very quickly.

Neogen delivers the kind of deep structural restoration and skin quality improvement that keeps clients coming back—and helps clinics grow faster.

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Certifications:

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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

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@artemisdistribution.com 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 (5litres/min) and flexible hose with releasable self-sealing valve connection to the generator.
Cylinder Pressure (Max) / Regulator Outlet Pressure 3000psi / 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 (4J, 2.5Hz)
B: With 25 mm disposable nozzle fitted, measured with a 25.0 +/-1mm 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 llb
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 Tyр.
(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 15.4ms
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 O 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.

DELIVERY

  • Shipping costs are calculated based on device size, weight, and destination.
  • Delivery is estimated within 1–3 months, depending on completion of the mandatory onboarding process.
  • After you place your order, our team will contact you to guide you through the Onboarding process:
    • Including device and contract support.
    • Business verification.
    • Contract completion.
    • Required training.

RETURNS

  • If your device arrives defective or damaged, notify us within 7 days of delivery with supporting evidence.
  • We will arrange a replacement. After 7 days, standard warranty terms apply.
  • Order cancellations before delivery are accepted, subject to a 10% restocking fee. Devices are not eligible for refund once delivered.
  • All returns are subject to approval and inspection.
  • Customers are responsible for return shipping costs.
  • To initiate a return, contact Artemis Support.

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

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@artemisdistribution.com 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 (5litres/min) and flexible hose with releasable self-sealing valve connection to the generator.
Cylinder Pressure (Max) / Regulator Outlet Pressure 3000psi / 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 (4J, 2.5Hz)
B: With 25 mm disposable nozzle fitted, measured with a 25.0 +/-1mm 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 llb
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 Tyр.
(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 15.4ms
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 O 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.

DELIVERY

  • Shipping costs are calculated based on device size, weight, and destination.
  • Delivery is estimated within 1–3 months, depending on completion of the mandatory onboarding process.
  • After you place your order, our team will contact you to guide you through the Onboarding process:
    • Including device and contract support.
    • Business verification.
    • Contract completion.
    • Required training.

RETURNS

  • If your device arrives defective or damaged, notify us within 7 days of delivery with supporting evidence.
  • We will arrange a replacement. After 7 days, standard warranty terms apply.
  • Order cancellations before delivery are accepted, subject to a 10% restocking fee. Devices are not eligible for refund once delivered.
  • All returns are subject to approval and inspection.
  • Customers are responsible for return shipping costs.
  • To initiate a return, contact Artemis Support.

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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.