Puregraft

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FAT GRAFTING

THE MOST PREDICTABLE FAT GRAFT ON THE MARKET.

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SURPASSING TRADITIONAL FAT TRANSFER PROCEDURES

Clinical research shows that using unstandardized fat grafting techniques can lead to 25-90% of the repurposed fat reabsorbed after the procedure. Excess of residual contaminants can promote inflammation and deliver unreliable outcomes.

SUPERIOR FAT

Puregraft is the only system that has been clinically validated in humans to improve long-term graft retention.

More than 97% of contaminants can be removed with the Puregraft system.

ENGINEERED FOR PERFECTION

Puregraft’s selective filtration technology is designed to gently dialyze harvested fat, removing only blood, oil, fluid, and fragmented cells within a closed system. This unique delivery system preserves the regenerative properties of fat. More than 97% of contaminants can be removed with the Puregraft system.

BETTER SYSTEM
BETTER RESULTS

Unlike traditional processing, Puregraft keeps fat tissue contained within a closed-system from start to finish, eliminating the risk of contamination.

SIMPLICITY DELIVERED

Along with its superior design Puregraft significantly saves time. As a result, providers can increase the number of patients treated per day.

Puregraft 4step

MORE ABOUT PUREGRAFT

  • Puregraft Before & After
  • Puregraft Before & After
  • Puregraft Before & After
  • Puregraft Before & After
  • Puregraft Before & After
  • Puregraft Before & After
  • Puregraft Before & After

WHITE PAPERS

Comparison of Three Fat Graft Preparation Methods: Gravity Separation, Centrifugation, and the Puregraft® System ›

Composition assessment of drained fluids in the Puregraft® Drain Bag ›

Long-Term Volumetric Retention of Autologous Fat Grafting Processed With Closed-Membrane Filtration ›

Facial Fat Grafting: Why, Where, How, and How Much ›

A Preliminary Assessment of the Predictability of Fat Grafting to Correct Silicone Breast Implant-Related Complications ›

PUREGRAFT IS THE ONLY CLINICALLY PROVEN, FDA CLEARED FAT-GRAFTING SYSTEM

  • Puregraft’s data-driven approach improves long-term retention and predictability while delivering a concentrated graft of healthy, viable fat cells
  • Closed system is ideal for large graft processing
  • Maintains the highest standards of sterility making the process safe
  • and consistent
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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.