Plasma IQ

THE FIRST FDA CLASS II CLEARED
HANDHELD PLASMA DEVICE

ENERGY-BASED RENEWAL

Plasma IQ is the latest advancement in aesthetics that delivers focused, controlled plasma energy to safely and effectively create microinjuries on the skin, renewing and restoring it. 

Microbeams of plasma are leveraged in a focused energy treatment, resulting in tightening and retraction of the skin tissues through controlled skin damage.

SAFE, QUICK AND EFFECTIVE

> Plasma IQ has a low risk of side effects. Extreme device precision and controlled energy settings limit the damage of surrounding skin, reduce downtime and improve healing.
> Plasma IQ treatment can be performed in-office in as little as 30 minutes, depending on the area(s) treated.
> Two levels of energy allow for safe and effective treatments for a variety of indications and areas. Plasma IQ delivers the precise amount of energy desired using the high (950V) or low (650V) settings during treatment.

THE FIRST FDA CLASS II

HANDHELD PLASMA DEVICE

PLASMA IQ IN ACTION

REAL RESULTS

HOW IT WORKS

IONIZED GAS PARTICLES As the device is brought close to the skin during treatment, it ionizes nitrogen gas particles in the air to create a plasma arc that looks like a spark. 

SKIN RETRACTION AND REACTION  The plasma arc causes sublimation of the epidermis of the skin; turning a solid into gas, resulting in immediate skin tightening and retraction in the target area. This method of plasma sublimation is highly targeted and controlled. It does not transfer heat to the surrounding area. 

The procedure creates tiny brown carbon crusts or scabs in the treated area that persist for approximately one week before dropping off. 

HEALING RESPONSE The microinjuries sustained during treatment promote the long-term firming, tightening, and smoothing effects that are part of the natural healing response.

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PLASMA IQ is FDA cleared to be used in the removal and destruction of skin lesions and the coagulation of tissue. The most common side effects are swelling, tenderness, scabbing and redness. PLASMA IQ is Rx only and should only be used by medically licensed and certified practitioners. For full product and safety information, visit https://www.sunevamedical.com/ifu/ ©2020 Neauvia North America

Important Safety Information

Bellafill®
Bellafill® is indicated for the correction of nasolabial folds and moderate to severe, atrophic, distensible facial acne scars on the cheek in patients over the age of 21 years. Patients who have had a positive reaction to the Bellafill® Skin Test, have a history of severe allergies, have known bovine collagen allergies, are allergic to lidocaine, have bleeding disorders or are prone to thick scar formation and/or excessive scarring should not receive Bellafill®. The safety of Bellafill® for use during pregnancy, breastfeeding, or in patients under 21 has not been established. You may experience temporary swelling, redness, pain, bruising, lumps/bumps, itching, and discoloration at the treatment site. These side effects are usually transient and typically resolve within 1–7 days. You may experience lumps/bumps/papules that may occur more than one month after injection and that may persist. Less common side effects include rash and itching more than 48 hours after treatment, persistent swelling or redness, lumps/bumps, acne, and increased sensitivity at treatment sites. Infrequently, granulomas may occur and may be treated by your licensed physician provider. Be sure to call your licensed provider immediately if you notice any unusual skin reactions around the treatment area. Based on the 5-year Post-Approval Study on nasolabial folds with 1,008 patients, long-term safety of Bellafill® for up to 5 years has been established.

PUREGRAFT
This product is certified as a medical device in the European Union under the Medical Device Directive 93/42/EEC by SGS CE0120, exclusively for the indication of autologous fat transfer. Other non-medical uses ascribed to this device such as aesthetic body contouring are not within the scope of CE certification, and users should be aware product performance and/or safety has not been evaluated by SGS for those purposes.

Suneva Medical HD PRP
REGULATORY STATUS: FDA-cleared 510(k) Class II medical device. Healeon HD PRP is designed to be used for the safe and rapid preparation of autologous platelet-rich-plasma (PRP) from a small sample of peripheral blood at the patient point of care. The PRP is mixed with autograft and/orallograft bone prior to application to a bony defect for improving handling characteristics. 510(k) number: BK170136

Silhouette Instalift
Silhouette lnstaLift® is indicated for use in mid-face suspension surgery to temporarily fixate the cheek sub-dermis in an elevated position.

IMPORTANT SAFETY CONSIDERATIONS
The Silhouette InstaLift device should not be used in patients with any known allergy or foreign body sensitivities to plastic/ biomaterial or in situations where internal fixation is otherwise contraindicated, (e.g. infection.) The device should also not be used in patients appearing to have very thin soft tissue of the face in which the implant may be visible or palpable.

Like all procedures of this type there is a possibility of adverse events, although not everybody experiences them. These adverse events include but are not limited to infection, minimal acute inflammatory tissue reaction, pain (which may be temporary or persistent in nature), swelling and edema, transient hematoma or bruising and transient rippling or dimple formation. For further safety or product information, please consult your physician.

For more safety information, please consult with your physician and the patient labeling that can be found by visiting our website www.bellafill.com.
Toll-free call (U.S. & Canada): 844-Bellafill (844-235-5234).
Local calls: 858-550-9999. International calls: ++ 858-550-9999.