It's Official...the Rejuvapen NXT is now FDA 510k Cleared!
AQ Skin Solutions formula is an innovative approach to harness healing. The AQ Skin Solutions formula consists of anti-inflammatory cytokines, interleukins, and growth factors.
AQ skin Solutions Growth Factor Technology was originally discovered through wound healing and cell regeneration therapy. Consistent medical research has proven that when formulated correctly, patented GF-technology holds the potential to boost the body's natural repair process.
AQ cosmeceutical serums contain conditioned media known to retain the highest quality of specific growth factors, cytokines, and interleukins that accelerate the regenerative process.
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.
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