Bellafill

BIOSTIMULATOR

THE ONLY FDA APPROVED 5-YEAR FILLER THAT STIMULATES PATIENT’S OWN NATURAL COLLAGEN.

THE “MUST-HAVE” PRODUCT FOR YOUR AESTHETIC PRACTICE

Bellafill is the only FDA approved filler that provides immediate correction and lasts up to 5 years with each treatment. Your patients are demanding a longer lasting alternative to their short acting HA fillers and only Bellafill can best address this need.

Addresses the #1 Patient Need – 90% of patients are interested in a 5-year dermal filler
Create Patient Loyalty with Bellafill – 82% of patients would switch providers for a 5-year filler
Use Bellafill to grow your practice beyond dermal fillers – 88% of patients would spend more money on other aesthetic procedures with the practice that provided them with a 5-year filler

Bellafill Approved

PROVEN SAFE AND EFFECTIVE

Bellafill is the most studied dermal filler on the market. With over 1,542 patients across multiple clinical studies, Bellafill has proven itself time and time again to be safe and effective. In fact, Bellafill’s 12-year Post Market Surveillance data shows a consistently low adverse event (0.12%) rate that is comparable to other HA fillers.

Bellafill Stimulates Collagen

IN A CLINICAL STUDY,

Bellafill was shown to stimulate both Type III and Type I – the ideal types of collagen for natural and long-lasting correction. The natural and long-lasting results are what give Bellafill it’s unprecedented patient satisfaction.

87% satisfaction rate in Bellafill’s 5-year clinical study
Rated the “Most Worth It” by actual patientson RealSelf

MORE ABOUT THE TECHNOLOGY
AND THE OPPORTUNITY

Bellafill increases patient loyalty and helps grow your filler practice and beyond.

Real patients. Real Results.

Hear what other providers are saying about Bellafill.

BECOME
A BELLAFILL
PROVIDER

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.