REJUVAPEN NXT® The NXT Evolution | Microneedling System | FDA 510k Cleared

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Rejuvenate Your Skin with the Rejuvapen NXT Microneedling Device

Microneedling is one the most popular aesthetic treatment today and helping drive this trend is Refine USA’s Rejuvapen NXT.

Our FDA-Cleared Rejuvapen NXT Microneedling System brings major technological advancements to the market with its 9 speed settings, precise infinite dial and brushless digital motor. Practitioners now have the flexibility to customize each patient’s treatments to produce consistent clinical results.

This innovative new technology can help improve skin’s appearance with little recovery time. As a result, the Rejuvapen is a perfect quick noninvasive procedure that delivers exceptional results.

Micronneedling Device Quality, Design and Performance

12,000 RPM
12 Stainless Steel, 33-Gauge ISO® Tips
Market-Leading Torque
Designed and Manufactured in the USA
Durable Medical-Grade Aluminum Design
Scalloped Edge Tip Eliminates Suction and Clogging
Plug-in System for Full-Power Treatments and Consistent Output
Ergonomic and Lightweight Design for Enhanced Comfort
Patent-Pending ISO® Seal

ISO™ Tips

Patent-Pending seal creates a barrier between tip and device.

 Smart Touch

Turn device on/off and adjust speed with ease using the digital fingertip control.

Infinite Dial

Control depth with the unique “infinite dial” for precise and customizable treatments, 0.01-2.5 mm.

Get in Touch with a Microneedling Expert

We're ready to lead you into the future of Aesthetics.

Dedicated to Safety

The Rejuvapen NXT continues to demonstrate its commitment to safety, quality, and excellence through safety testing. As a market leader, Rejuvapen has performed over 500,000 safe and effective treatments.

Life Cycle Testing (Cleaning & Disinfection)
ISO Seal Integrity Testing and Process Validation
CE Mark

AAMI / IEC 60601-1-2: 2004 Electromagnetic Compatibility, Immunity, Emissions, and Essential Performance Testing

EN 60601-1: 2006 + A1: 2013 Electrical Safety Testing
ES 60601-1: 2005 + C1 (2009) + A1 (2010) + A2 (2010) Electrical Safety Testing

FDA 510k Cleared: K192138

Tested for Quality and Safety

FDA 510k Cleared and Trusted by thousands of Aesthetic Practitioners

Quick Processing and Ship Times

Schedule a Demo Today!

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