Resources

Regional Training Centers

Suneva Medical supports these professional, licensed providers with expertise in Bellafill® to offer Bellafill® Product Training. Clinical Training is provided to support clinical proficiency with Bellafill® utilization in clinical practice. These trainings are designed for the expert, experienced and licensed injector who is ready to offer a long-lasting solution for facial rejuvenation to patients.

To learn more about or find a Regional Training Center please use the search functionality below.

       

      LEARN MORE ABOUT OUR REGIONAL TRAINING CENTERS

      Aesthetic Clinical Trainers

      Candy Morrow

      Candy Morrow RN – Brookhaven, GA

      Candy began her nursing career in 1979, working in acute care. She owned and operated a Home Infusion Company for over ten years, providing intravenous pharmaceutical services to individuals in their homes. In 2006, she pursed her passion for aesthetics and received advanced aesthetic injector training certifications. Candy brings with her 12 years of advanced injector aesthetic experience.

      Jennifer Baker

      Jennifer Baker RN, BSN – Austin, TX

      BS in Nursing, Chamberlain University

      Owned a Cosmetic Surgery Center/Medical Spa for 10 years. Injecting for 15 years and training for 8 years.

      John DelRossi

      John DelRossi PA – Orange County, CA

      BS in Accounting, Rowan University and BS in Allied Health, MCP Hahnemann University

      20 years as a Physician Assistant (started in internal medicine) with 15 years in aesthetic care. Advanced injector of neuromodulators and facial fillers. One of the first in the nation (and remains one of the largest) to treat HIV related lipoatrophy. Leading expert on long term fillers.

      Justine Roberts

      Justine Roberts PA – Cresson, PA

      Master Physician Assistant Science, Saint Francis University

      Began practicing in 2009, with 8 years experience as a Plastic Surgery Physician Assistant. Chose to focus her practice on Aesthetic Medicine/Cosmetic Dermatology. Education consultant for an Aesthetic Medical Education company, as well as an Adjunct Instructor at Saint Francis University in the Physician Assistant Science and Public Health Programs.

      Shannon Foley RN, BSN – Berlin, Maryland

      Master Aesthetic Injector, Aesthetic Nurse Specialist

      14 years experience in the art and science of aesthetic injectables. She has extensive experience as an Aesthetic Clinical Trainer beginning with formerly BioForm and Merz North America in 2006.  Shannon continues to see her aesthetic injectable patients and is currently using Bellafill in her practice.

      Andrea Tankersley RN, BSN – Colorado Springs, CO

      Master Aesthetic Injector, Aesthetic Nurse Specialist

      Andrea began her aesthetic career in 1998 while working for a dermatologist. With a desire to broaden her knowledge and skills, she went on to work for a plastic surgeon for 9 years. She discovered her passion for sharing her knowledge and experience with dermal fillers and neuromodulators. She spent the next 8 years helping fellow providers deliver safe and beautiful outcomes to their patients in both a clinical educator and Medical Science Liaison capacity. During this time, she continued to see her own clients while working for an oculoplastic surgeon in Colorado Springs.

       

      LEARN MORE ABOUT OUR AESTHETIC CLINICAL TRAINERS

      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.