Neogen

The #1 “Ozempic Face” Solution. Restore volume and treat structural skin regeneration for the surging post-weight loss patient demographic.

Address the “Ozempic Face” and skin laxity epidemic with a clinical partnership that guarantees your growth. Access a monthly Launch Fund ($1,300) to protect your cash flow for 12 months, secured by a guaranteed payback by month 13.

Neogen is the ultimate non-invasive solution for structural skin regeneration—trusted worldwide and FDA-cleared for professional use.

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LAUNCH REBATE

Access a $1,300/mo Launch Rebate for 12 months to protect your cash flow while you scale your results. This consistent financial injection reduces overhead pressure, allowing you to focus entirely on client care and results.

COMPLIMENTARY NOZZLES

Every Neogen system includes two boxes of genuine plasma nozzles valued at over $5,000. This inventory eliminates initial consumable overhead, maximizing profit on your first wave of patients.

PROFIT GUARANTEE

Eliminate investment risk with a contractually backed guarantee to reach profitability by month 13 or we pay the difference. Our commitment to your clinical success is absolute, providing a safety net that protects your bottom line.

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.
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.