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U.S. manufacturing facility

018 · Device

AuraGraft.

Developed by the original team that introduced suction-assisted FUE globally, AuraGraft is built to optimize safety, precision, and clinical outcomes. Lightweight (just 38 lbs), portable, and durable, it’s backed by an industry-leading 3-year warranty—setting a new standard for reliability in hair restoration.

AuraGraft FUE hair transplant console with touchscreen, collection canister, and handpiece
Cryogenic vials in a U.S. laboratory

QBio

“QBio. Documented lots. FDA-cleared topical-use cosmetics. Not a brochure.”

United States · Professional use

50B
Exosome-sized particles per vial (Elixir, Gro)
FDA
Cleared for topical use
U.S.
Manufactured in an FDA-registered facility

The difference

Three sentences we will not say.

  • 01

    That it belongs in a joint

    We will not market QBio as a treatment for a joint. Documentation is not a wink.

  • 02

    That Gro is a growth drug

    It is a professional scalp cosmetic. Hair restoration is a diagnosis, a camera, and a device — not a vial.

  • 03

    That it is FDA approved

    QBio is an FDA-cleared topical-use product. We will not say approved when the labeling says cleared.

Practice inquiry

A conversation with the desk.

The catalog. Licensed practices only. No patient details, please.