Plain-English version of what we do, what we don't do, and what FDA clearance actually means.
The Neubie is an FDA-cleared Class II direct-current neuromuscular electrical stimulation device, manufactured by NeuFit. "FDA-cleared" means the device has been determined by the U.S. Food and Drug Administration to be substantially equivalent to a legally marketed predicate device and may be marketed for specific therapeutic indications. It is NOT the same thing as FDA-approved drug therapy.
The Neubie is indicated for:
The Neubie is contraindicated for patients with:
Additional caution is appropriate for patients with active malignancy, severe cardiac conditions, recent unstable injuries, open wounds in the treatment area, or active bleeding disorders. All patients are screened at intake before their first session.
Per the device manufacturer's commercial-use policy and applicable state regulations, the Neubie may only be used commercially by a licensed practitioner whose scope of practice covers electrical modalities, or under that practitioner's supervision. All Neubie sessions at Lexis Peptora are delivered under the on-premises supervision of a licensed chiropractor of record. Trainers and chiropractic assistants who operate the device do so under that supervision and have completed NeuFit Level 1 certification plus state-required assistant training.
The Neubie is non-invasive and generally safe within its FDA-cleared indications. That said, if you are unsure whether the Neubie is appropriate for your condition, you should consult your physician before booking. Specifically consult a physician before treatment if you have:
This disclaimer is effective as of 2026-05-25 and may be updated. We will post the date of any future updates here.