The NXT Evolution
FDA Cleared Microneedling
Made in the USA
Call Today for a free Demo!
The Rejuvapen System utilizes an array of stainless steel needle cartridges. This innovative new technology can help improve your appearance with little recovery time. As a result, the Rejuvapen is a perfect noninvasive lunchtime procedure that delivers exceptional results.
The Rejuvapen NXT continues to demonstrate its commitment to safety, quality and excellence through safety testing. As a market leader, the Rejuvapen has performed over 500,000 safe and effective treatments.
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
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Patent Pending Tips with ISO Seal Creates Barrier Between
The Tip and The Device.
Digital Control, Equipped
with 9 Speed Settings.
The Rejuvapen NXT adjusts for precise treatments from 0.2-2.5 mm.
Regulatory Status: The PureSpin is an FDA cleared 510 (K) Class II medical device. PureSpin PRP® is intended for the safe and rapid preparation of autologous platelet-rich plasma (PRP) from a small sample of blood at the patient point of care. The PRP is mixed with autograph or allograft bone prior to application to an orthopedic surgical site. 510 (K ) number BK050055. The Rejuvapen® is marketed for and has an intended use for micro-pigmentation treatments. The Apex Magnum® has an intended use as a Therapeutic massager under Sec. 890.5660. A therapeutic massager is an electrically powered device intended for medical purposes, such as to relieve minor muscle aches and pains.The Rejuvapen NXT ® is marketed for and has an intended use as a micro-pigmentation treatments. Copyright © 2018 Refine USA - All Rights Reserved.